LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II— 510(k) K865014

Name: FDA 510(k) clearance K865014
Creator: U.S. Food and Drug Administration
Published: 1987-01-09

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K865014 for LIQUICHEK IMMUNOLOGY CONTROL (HUMAN) LEVELS I & II, Substantially Equivalent on 1987-01-09. Applicant: Bio-Rad. Device class: 1.

Clearance details

Applicant: Bio-Rad
Product code: Code DGR
Device class: Class 1
Regulation: 21 CFR 866.5700
Advisory panel: Immunology
Date received: 1986-12-23
Decision date: 1987-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, CA, US

Download summary PDF View on FDA.gov ↗

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