LIQUICHEK RHEUMATOID FACTOR CONTROL— 510(k) K960987

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K960987 for LIQUICHEK RHEUMATOID FACTOR CONTROL, Substantially Equivalent on 1996-06-04. 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: 1996-03-11
Decision date: 1996-06-04
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.