LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573— 510(k) K002120

Name: FDA 510(k) clearance K002120
Creator: U.S. Food and Drug Administration
Published: 2000-08-21

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K002120 for LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573, Substantially Equivalent on 2000-08-21. Applicant: Bio-Rad. Device class: 1.

Clearance details

Applicant: Bio-Rad
Product code: Code JJS
Device class: Class 1
Regulation: 21 CFR 862.1660
Advisory panel: Clinical Chemistry
Date received: 2000-07-13
Decision date: 2000-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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