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

RHEUMA-CHECK ENZYME IMMUNOASSAY TEST

K Number: K871196 · Decision May 6, 1987
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
28
Review Days
43

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Basic Information

Device Name
RHEUMA-CHECK ENZYME IMMUNOASSAY TEST
K Number
K871196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Orion Diagnostica, Inc.
Date Received
March 24, 1987
Decision Date
May 6, 1987
Product Code
DHR
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
DHR System, Test, Rheumatoid Factor

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Other Clearances by Orion Diagnostica, Inc.

K Number Device Name
K942286 DIARLEX ROTA-ADENO
K914892 SALIVA-STIM
K904655 PYLORISET
K884074 IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN G
K884147 IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN M
K884075 IMMUNOCHEMICAL DETERMINATION OF TRANSFERRIN
K884040 IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN A
K864645 ADENOLEX (R) LATEX AGGLUTINATION TEST
K862475 RESPIRASTICK ENZYME IMMUNOASSAY TEST
K854129 ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS
Search all 28 clearances from Orion Diagnostica, Inc. →