LIQUICHEK DIABETES CONTROL, LEVEL 1,2,3,4— 510(k) K052838

Name: FDA 510(k) clearance K052838
Creator: U.S. Food and Drug Administration
Published: 2005-11-09

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K052838 for LIQUICHEK DIABETES CONTROL, LEVEL 1,2,3,4, Substantially Equivalent on 2005-11-09. Applicant: Bio-Rad. Device class: 2.

Clearance details

Applicant: Bio-Rad
Product code: Code GGM
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 2005-10-07
Decision date: 2005-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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