FIDIS CONNECTIVE 8— 510(k) K050286

Name: FDA 510(k) clearance K050286
Creator: U.S. Food and Drug Administration
Published: 2005-10-03

Substantially Equivalent

Biomedical Diagnostics (Bmd) SA

FDA 510(k) clearance K050286 for FIDIS CONNECTIVE 8, Substantially Equivalent on 2005-10-03. Applicant: Biomedical Diagnostics (Bmd) SA. Device class: 2.

Clearance details

Applicant: Biomedical Diagnostics (Bmd) SA
Product code: Code LLL
Device class: Class 2
Regulation: 21 CFR 866.5100
Advisory panel: Immunology
Date received: 2005-02-07
Decision date: 2005-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marne La Vallee Cedex 2, FR

Download summary PDF View on FDA.gov ↗

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