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

ORICULT DTM

K Number: K802947 · Decision Dec 22, 1980
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
284
Applicant Total
28
Review Days
33

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Basic Information

Device Name
ORICULT DTM
K Number
K802947
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2360
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Orion Diagnostica, Inc.
Date Received
November 19, 1980
Decision Date
December 22, 1980
Product Code
JSI
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
JSI Culture Media, Selective And Differential

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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
K862475 RESPIRASTICK ENZYME IMMUNOASSAY TEST
Search all 28 clearances from Orion Diagnostica, Inc. →