LIQUICHEK RHEUMATOID FACTOR CONTROL— 510(k) K923578

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K923578 for LIQUICHEK RHEUMATOID FACTOR CONTROL, Substantially Equivalent on 1992-10-06. Applicant: Bio-Rad. Device class: 2.

Clearance details

Applicant: Bio-Rad
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1992-07-20
Decision date: 1992-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, 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.