BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM— 510(k) K942451

Name: FDA 510(k) clearance K942451
Creator: U.S. Food and Drug Administration
Published: 1994-11-10

Substantially Equivalent

Bio-Rad

FDA 510(k) clearance K942451 for BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM, Substantially Equivalent on 1994-11-10. Applicant: Bio-Rad. Device class: 1.

Clearance details

Applicant: Bio-Rad
Product code: Code LDM
Device class: Class 1
Regulation: 21 CFR 862.2260
Advisory panel: Clinical Chemistry
Date received: 1994-05-23
Decision date: 1994-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hercules, CA, US

Download summary PDF View on FDA.gov ↗

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