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

DIRECT ESTRIOL RIA KIT

K Number: K781546 · Decision Dec 4, 1978
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
41
Applicant Total
50
Review Days
82

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Basic Information

Device Name
DIRECT ESTRIOL RIA KIT
K Number
K781546
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1265
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Immunalysis Corporation
Date Received
September 13, 1978
Decision Date
December 4, 1978
Product Code
CGI
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
CGI Radioimmunoassay, Estriol

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