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

IN VITRO FERRITIN RIA TEST

K Number: K770702 · Decision Jun 17, 1977
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
27
Review Days
60

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Basic Information

Device Name
IN VITRO FERRITIN RIA TEST
K Number
K770702
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Clinical Assays, Inc.
Date Received
April 18, 1977
Decision Date
June 17, 1977
Product Code
DBF
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
DBF Ferritin, Antigen, Antiserum, Control

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K Number Device Name
K832711 VITAMIN B12 FOLATE CA-1515-125
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K832710 VITAMIN B12 RADIOASSAY KIT CA-1534
K823476 GAMMADAB LH RADIO-KIT #CA-1508
K823313 IN VITRO GAMMACOAT B-HCG RADIO. TEST
K821611 GAMMADAB [125] FSH RADIOIMMUNAY KIT
K821092 GAMMADAB[125]EGE RADIOIMMUNOASSAY IT
K812227 GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY
K810722 GASTRIN RADIOIMMUNOASSAY TEST
K810967 IN-VITRO TBG RADIOIMMUNOASSAY TEST
Search all 27 clearances from Clinical Assays, Inc. →