FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RESPIRASTICK ENZYME IMMUNOASSAY TEST

K Number: K862475 · Decision Sep 16, 1986
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
28
Review Days
78

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Basic Information

Device Name
RESPIRASTICK ENZYME IMMUNOASSAY TEST
K Number
K862475
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Orion Diagnostica, Inc.
Date Received
June 30, 1986
Decision Date
September 16, 1986
Product Code
GTY
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GTY Antigens, All Groups, Streptococcus Spp.

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GTY), ordered by most recent decision date.

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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
K871196 RHEUMA-CHECK ENZYME IMMUNOASSAY TEST
K854129 ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS
Search all 28 clearances from Orion Diagnostica, Inc. →