RADIOIMMUNOASSAY KIT(CORTISOL IN PLASMA)— 510(k) K761346

Name: FDA 510(k) clearance K761346
Creator: U.S. Food and Drug Administration
Published: 1977-01-07

Substantially Equivalent

New England Nuclear

FDA 510(k) clearance K761346 for RADIOIMMUNOASSAY KIT(CORTISOL IN PLASMA), Substantially Equivalent on 1977-01-07. Applicant: New England Nuclear. Device class: 2.

Clearance details

Applicant: New England Nuclear
Product code: Code CGR
Device class: Class 2
Regulation: 21 CFR 862.1205
Advisory panel: Clinical Chemistry
Date received: 1976-12-28
Decision date: 1977-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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