RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL— 510(k) K862871

Name: FDA 510(k) clearance K862871
Creator: U.S. Food and Drug Administration
Published: 1986-08-19

Substantially Equivalent

Cambridge Medical Technology

FDA 510(k) clearance K862871 for RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL, Substantially Equivalent on 1986-08-19. Applicant: Cambridge Medical Technology. Device class: 2.

Clearance details

Applicant: Cambridge Medical Technology
Product code: Code CGR
Device class: Class 2
Regulation: 21 CFR 862.1205
Advisory panel: Clinical Chemistry
Date received: 1986-07-29
Decision date: 1986-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Billerica, MA, US

Download summary PDF View on FDA.gov ↗

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