Atlas FDA

ASSERACHROM PF4 KIT

FDA 510(k) clearance K862774 · decided 1986-09-04

Clearance details

K-number
K862774
Device name
ASSERACHROM PF4 KIT
Applicant
American Bioproducts Co.
Decision
Substantially Equivalent
Date received
1986-07-22
Decision date
1986-09-04
Days to decision
44 days
Clearance type
Traditional
Product code
LCO
Device class
2
Regulation number
864.7695
Medical specialty
Hematology
Advisory committee
Hematology
Location
Parsippany, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
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HemosIL AcuStar HIT-IgG(PF4-H), HemosIL AcuStar HIT Controls (K170854)Instrumentation Laboratory CO2017-09-08
HemosIL HIT-Ab(PF4-H), HemosIL HIT-Ab(PF4-H) Controls (K153137)Instrumentation Laboratory CO2016-07-08
PF4 IGG (K071781)Genetic Testing Institute2007-12-19
ZYMUTEST HIA IGGAM, ZYMUTEST IGG, MODEL RK040D, RK040A (K071255)Hyphen Biomed2007-09-07
PF4 ENHANCED SOLID PHASE ELISA (K053559)Genetic Testing Institute2006-01-20
HEALTHTEST HEPARIN/PLATELET FACTOR 4 ANTIBODY ASSAY (K040293)Akers Laboratories, Inc.2004-05-28
ASSERACHROM HPIA TEST KIT (K003767)Diagnostica Stago, Inc.2001-02-12
GTI-PF4 ELISA (K983379)Genetic Testing Institute1999-03-09
ENZYGNOST PLATELET FACTOR 4 (PF4) KIT (K890633)Behring Diagnostics, Inc.1989-04-21

Recalls involving this device

No recalls on record reference this clearance.