RIA KIT, GAMMADAB ESTRIOL— 510(k) K781938

Name: FDA 510(k) clearance K781938
Creator: U.S. Food and Drug Administration
Published: 1979-01-10

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K781938 for RIA KIT, GAMMADAB ESTRIOL, Substantially Equivalent on 1979-01-10. Applicant: Clinical Assays, Inc.. Device class: 1.

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code CGI
Device class: Class 1
Regulation: 21 CFR 862.1265
Advisory panel: Clinical Chemistry
Date received: 1978-11-20
Decision date: 1979-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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