LIQUICHEK RETICULOCYTE CONTROL (A)— 510(k) K042836

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K042836 for LIQUICHEK RETICULOCYTE CONTROL (A), Substantially Equivalent on 2004-11-05. Applicant: Bio-Rad. Device class: 2.

Clearance details

Applicant: Bio-Rad
Product code: Code JPK
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 2004-10-14
Decision date: 2004-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.