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

GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY

K Number: K812227 · Decision Sep 24, 1981
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
26
Applicant Total
27
Review Days
45

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Basic Information

Device Name
GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY
K Number
K812227
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1405
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Clinical Assays, Inc.
Date Received
August 10, 1981
Decision Date
September 24, 1981
Product Code
CFP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CFP Radioimmunoassay, Immunoreactive Insulin

Similar 510(k) Clearances

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Other Clearances by Clinical Assays, Inc.

K Number Device Name
K832711 VITAMIN B12 FOLATE CA-1515-125
K832712 FOLATE RADIOASSAY KIT CA-1562-125
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
K810722 GASTRIN RADIOIMMUNOASSAY TEST
K810967 IN-VITRO TBG RADIOIMMUNOASSAY TEST
K801667 GAMMA COAT(125 I) RUBELLA ANTIBODY
Search all 27 clearances from Clinical Assays, Inc. →