MR1 LUTROPIN RIA KIT— 510(k) K820741

Name: FDA 510(k) clearance K820741
Creator: U.S. Food and Drug Administration
Published: 1982-04-14

Substantially Equivalent

Microanalytic Research, Inc.

FDA 510(k) clearance K820741 for MR1 LUTROPIN RIA KIT, Substantially Equivalent on 1982-04-14. Applicant: Microanalytic Research, Inc.. Device class: 1.

Clearance details

Applicant: Microanalytic Research, Inc.
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1982-03-18
Decision date: 1982-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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