CENTRIA CORTISOL RIA— 510(k) K771117

Name: FDA 510(k) clearance K771117
Creator: U.S. Food and Drug Administration
Published: 1977-06-23

Substantially Equivalent

Clinical Diagnostics, Inc.

FDA 510(k) clearance K771117 for CENTRIA CORTISOL RIA, Substantially Equivalent on 1977-06-23. Applicant: Clinical Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Clinical Diagnostics, Inc.
Product code: Code CGR
Device class: Class 2
Regulation: 21 CFR 862.1205
Advisory panel: Clinical Chemistry
Date received: 1977-06-21
Decision date: 1977-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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