FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

IMMUNOCHEMICAL DETERMINATION OF TRANSFERRIN

K Number: K884075 · Decision Oct 19, 1988
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
28
Review Days
22

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Basic Information

Device Name
IMMUNOCHEMICAL DETERMINATION OF TRANSFERRIN
K Number
K884075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5880
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Orion Diagnostica, Inc.
Date Received
September 27, 1988
Decision Date
October 19, 1988
Product Code
DDG
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
DDG Transferrin, Antigen, Antiserum, Control

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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
K884040 IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN A
K864645 ADENOLEX (R) LATEX AGGLUTINATION TEST
K871196 RHEUMA-CHECK ENZYME IMMUNOASSAY TEST
K862475 RESPIRASTICK ENZYME IMMUNOASSAY TEST
K854129 ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS
Search all 28 clearances from Orion Diagnostica, Inc. →