CORTISOL RADIOIMMUNOASSAY SYSTEM— 510(k) K792036

Name: FDA 510(k) clearance K792036
Creator: U.S. Food and Drug Administration
Published: 1979-10-30

Substantially Equivalent

Radioimmunoassay, Inc.

FDA 510(k) clearance K792036 for CORTISOL RADIOIMMUNOASSAY SYSTEM, Substantially Equivalent on 1979-10-30. Applicant: Radioimmunoassay, Inc.. Device class: 2.

Clearance details

Applicant: Radioimmunoassay, Inc.
Product code: Code CGR
Device class: Class 2
Regulation: 21 CFR 862.1205
Advisory panel: Clinical Chemistry
Date received: 1979-10-11
Decision date: 1979-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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