GASTRIN RADIOIMMUNOASSAY TEST— 510(k) K810722

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K810722 for GASTRIN RADIOIMMUNOASSAY TEST, Substantially Equivalent on 1981-05-27. Applicant: Clinical Assays, Inc..

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code CGC
Advisory panel: Clinical Chemistry
Date received: 1981-03-17
Decision date: 1981-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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