18 results
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30ms
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Sources: EU EUDAMED, US FDA
ACCUMETRICS,INC. VERIFYNOW PRUTEST, ACCUMETRICS, INC. VERIFYNOW PRUTEST
FDA 510(k)
FDA Class 2
·Hematology
ULTEGRA RPFA-TRAP
FDA Adverse Event
Malfunction
·ACCUMETRICS INC.·Product code JOZ·October 10, 2000
VerifyNow System, part #85005-6H Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade. The VerifyNow Systems intended for use with human whole blood and verify now test devices. The system should be operated by healthcare professionals trained on use of the system and in accordance with institution and policies and procedures. Accumetrics respresentatives will assist your institution in the installation of the system and operations of the operator.
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·February 6, 2012
VerifyNow P2Y12 Assay, Part Number: 85064, All reagent lots. Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade. The VerifyNow Systems intended for use with human whole blood and verify now test devices. The system should be operated by healthcare professionals trained on use of the system and in accordance with institution and policies and procedures. Accumetrics respresentatives will assist your institution in the installation of the system and operations of the operator.
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·February 6, 2012
HEMOCHRON SIGNATURE ELITE
FDA Adverse Event
Malfunction
·ACCRIVA DIAGNOSTIC INC., DBA INC, DBA ACCUMETRICS·Product code JPA·February 12, 2018
HEMOCHRON
FDA Adverse Event
Malfunction
·ACCRIVA DIAGNOSTICS INC., DBA ITC, DBA ACCUMETRICS·Product code JPA·September 18, 2015
ACT+ CUVETTE
FDA Adverse Event
ACCRIVA DIAGNOSTICS INC., DBA ITC, DBA ACCUMETRICS·Product code JBP·June 1, 2015
VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or eptifibatide. VerifyNow lIb/IlIa Test results should be interpreted in conjunction with other clinical and laboratory data available to the clinician. The VerifyNow System is a turbidimetric based optical detection system which measures platelet-induced aggregation. The system consists of an instrument, a disposable test device and quality control materials. The VerifyNow lIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or eptifibatide.
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·November 14, 2013
VerifyNow P2Y12 Assay Device Kit, Part Number 85054
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·September 5, 2006
VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011, 25-Test kit. Product Usage: The VerifyNow System is a turbidimetric based optical detection system which measures platelet-induced aggregation. The system consists of an instrument, a disposable test device and quality control materials. The VerifyNow IIb/IIIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) IIb/IIIa receptor blockade in patients treated with abciximab or eptifibatide. VerifyNow Ilb/Illa Test results should be interpreted in conjunction with other clinical and laboratory data available to the clinician.
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·February 13, 2014
VerifyNow Asprin Assay Kit Part No. 85034
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·May 10, 2004
Accumetrics part number 29001 VerifyNow Instrument, printe power supply
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·September 13, 2005
VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or eptifibatide. VerifyNow lIb/IlIa Test results should be interpreted in conjunction with other clinical and laboratory data available to the clinician. The VerifyNow System is a turbidimetric based optical detection system which measures platelet-induced aggregation. The system consists of an instrument, a disposable test device and quality control materials. The VerifyNow lIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or eptifibatide.
FDA Enforcement
Class II
·Terminated·Accumetrics Inc·December 18, 2013
VerifyNow System, part #85005-6H Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade. The VerifyNow Systems intended for use with human whole blood and verify now test devices. The system should be operated by healthcare professionals trained on use of the system and in accordance with institution and policies and procedures. Accumetrics respresentatives will assist your institution in the installation of the system and operations of the operator.
FDA Enforcement
Class II
·Terminated·Accumetrics Inc·June 27, 2012
VerifyNow P2Y12 Assay, Part Number: 85064, All reagent lots. Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade. The VerifyNow Systems intended for use with human whole blood and verify now test devices. The system should be operated by healthcare professionals trained on use of the system and in accordance with institution and policies and procedures. Accumetrics respresentatives will assist your institution in the installation of the system and operations of the operator.
FDA Enforcement
Class II
·Terminated·Accumetrics Inc·June 27, 2012
VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011, 25-Test kit. Product Usage: The VerifyNow System is a turbidimetric based optical detection system which measures platelet-induced aggregation. The system consists of an instrument, a disposable test device and quality control materials. The VerifyNow IIb/IIIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) IIb/IIIa receptor blockade in patients treated with abciximab or eptifibatide. VerifyNow Ilb/Illa Test results should be interpreted in conjunction with other clinical and laboratory data available to the clinician.
FDA Enforcement
Class II
·Terminated·Accumetrics Inc·March 19, 2014
Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.
FDA Recall
Terminated
·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·Product code JPA·April 22, 2016
Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.
FDA Enforcement
Class II
·Terminated·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·June 1, 2016