LIQUICHEK(R) SERUM ALCOHOL CONTROL; LEVELS 1,2 & 3— 510(k) K892004

Name: FDA 510(k) clearance K892004
Creator: U.S. Food and Drug Administration
Published: 1989-04-21

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K892004 for LIQUICHEK(R) SERUM ALCOHOL CONTROL; LEVELS 1,2 & 3, Substantially Equivalent on 1989-04-21. Applicant: Bio-Rad. Device class: 1.

Clearance details

Applicant: Bio-Rad
Product code: Code LAS
Device class: Class 1
Regulation: 21 CFR 862.3280
Advisory panel: Clinical Toxicology
Date received: 1989-03-28
Decision date: 1989-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hercules, CA, US

Download summary PDF View on FDA.gov ↗

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