FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACT CONTROL SET

K Number: K940840 · Decision Jul 19, 1994
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
164
Review Days
146

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Basic Information

Device Name
ACT CONTROL SET
K Number
K940840
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sigma Diagnostics, Inc.
Date Received
February 23, 1994
Decision Date
July 19, 1994
Product Code
JPA
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JPA System, Multipurpose For In Vitro Coagulation Studies

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Other Clearances by Sigma Diagnostics, Inc.

K Number Device Name
K021162 AMAX DENSITY COAGULATION ANALYZER, AMAX DENSTINY COAGULATION ANALYZER-EU, AMAX DESTINY COAGULATION ANALYZER-REFURBISHED
K020109 SIGMA DIAGNOSTICS ACCUCLOT LA CONTROL
K013549 SIGMA DIAGNOSTICS AUTO D-DIMER CALIBRATOR, MODEL A7971
K013544 SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 2, MODEL A8096
K013545 SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 3, MODEL A8221
K012410 INFINITY HBA KIT, MODELS 537-A, 537-B
K010652 SIGMA DIAGNOSTICS SIGMA-CAL, MODEL S2936
K010158 THROMBOMAX-HS WITH CALCIUM, MODEL T6540
K003267 SIGMA DIAGNOSTICS AUTO D-DIMER, MODEL CRS126-A
K003329 SIGMA DIANOSTICS AUTO D-DIMER CONTROL LEVEL 2, MODEL A5217
Search all 164 clearances from Sigma Diagnostics, Inc. →