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

ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE

K Number: K802404 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
36
Applicant Total
24
Review Days
17

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Basic Information

Device Name
ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE
K Number
K802404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5040
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Ortho Diagnostics, Inc.
Date Received
October 6, 1980
Decision Date
October 23, 1980
Product Code
DCF
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DCF Albumin, Antigen, Antiserum, Control

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Other Clearances by Ortho Diagnostics, Inc.

K Number Device Name
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
K781860 ASSAY, CHROMOGENIC ANTITHROMBIN III
Search all 24 clearances from Ortho Diagnostics, Inc. →