LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAY— 510(k) K132227

Substantially Equivalent

Bio-Rad Laboratories

FDA 510(k) clearance K132227 for LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAY, Substantially Equivalent on 2013-10-25. Applicant: Bio-Rad Laboratories. Device class: 1.

Clearance details

Applicant
Bio-Rad Laboratories
Product code
Code JJY
Device class
Class 1
Regulation
21 CFR 862.1660
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Irvine, CA, US
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