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

PLASMA COAGULATION CONT., ABNORMAL

K Number: K781104 · Decision Aug 10, 1978
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
51
Applicant Total
24
Review Days
38

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Basic Information

Device Name
PLASMA COAGULATION CONT., ABNORMAL
K Number
K781104
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7925
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Ortho Diagnostics, Inc.
Date Received
July 3, 1978
Decision Date
August 10, 1978
Product Code
GFO
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
GFO Activated Partial Thromboplastin

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Other Clearances by Ortho Diagnostics, Inc.

K Number Device Name
K802404 ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE
K801507 ANTIGEN CONTROL CELLS
K800357 BI-LEVEL ASSAYED CARD. DRUG CONT., I,II
K800310 ORTHO ANTISERA CONTROL
K791791 ORTHO ANTIBODY ENHANCEMENT SOLUTION
K791301 ORTHO TSH RIA KIT
K790813 MULTECON BLOOD GAS CONTROL
K782063 PREGNANCY, SENSIDEX TUBE TEST
K782166 SLIDE TEST FOR PREGNANCY, GRAVINDEX 90
K781638 RUBINDEX*DIRECT SYSTEM
Search all 24 clearances from Ortho Diagnostics, Inc. →