QUANTIMUNE HLH RIA HUMAN LUTENIZING HORM— 510(k) K810302

Name: FDA 510(k) clearance K810302
Creator: U.S. Food and Drug Administration
Published: 1981-02-25

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K810302 for QUANTIMUNE HLH RIA HUMAN LUTENIZING HORM, Substantially Equivalent on 1981-02-25. Applicant: Bio-Rad. Device class: 1.

Clearance details

Applicant: Bio-Rad
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1981-02-05
Decision date: 1981-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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