DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI— 510(k) K822298

Name: FDA 510(k) clearance K822298
Creator: U.S. Food and Drug Administration
Published: 1982-09-02

Substantially Equivalent

Nuclear Medical Laboratories, Inc.

FDA 510(k) clearance K822298 for DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI, Substantially Equivalent on 1982-09-02. Applicant: Nuclear Medical Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Nuclear Medical Laboratories, Inc.
Product code: Code JFH
Device class: Class 2
Regulation: 21 CFR 862.1020
Advisory panel: Clinical Chemistry
Date received: 1982-08-03
Decision date: 1982-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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