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

STA - VWF CONTROL [N]+[P] KIT

K Number: K962674 · Decision Jul 23, 1996
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
98
Applicant Total
79
Review Days
14

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Basic Information

Device Name
STA - VWF CONTROL [N]+[P] KIT
K Number
K962674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Bioproducts Co.
Date Received
July 9, 1996
Decision Date
July 23, 1996
Product Code
GGN
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
GGN Plasma, Coagulation Control

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Other Clearances by American Bioproducts Co.

K Number Device Name
K983460 STAR AUTOMATED MULTI-PARAMETRIC ANALYZER
K971519 ASSERACHROM TPA TEST KIT
K964716 STA LIATEST CONTROL [N]+[P] KIT
K964728 STA-LIATEST D-DI TEST KIT
K964718 STA D-DI CALIBRATOR KIT
K962675 STA - LIATEST VWF TEST KIT
K962671 STA-VWF CALIBRATOR KIT
K961579 STA COMPACT AUTOMATED MULTI-PARAMETRIC ANALYZER
K955040 AT-III CONTROL PLASMA KIT
K954040 ASSERACHROM TOTAL PROTEIN S KIT
Search all 79 clearances from American Bioproducts Co. →