10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COLLAGUARD, MODEL FCIA,FCIB,FCIC,AND FCID
FDA 510(k)
FDA Unclassified
·Unknown
LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM (FAMILY OF PRODUCTS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MB 11
FDA 510(k)
FDA Class 2
·Neurology
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·March 29, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·April 18, 2011
NXSTAGE SYSTEM ONE
FDA Adverse Event
Malfunction
·NXSTAGE MEDICAL, INC.·Product code KDI·June 13, 2008
BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Company·July 26, 2017
BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Company·July 26, 2017
BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Company·July 26, 2017
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.
FDA Enforcement
Class II
·Terminated·Smiths Medical ASD, Inc.·June 24, 2015