BECE PRESS— 510(k) K090434

Name: FDA 510(k) clearance K090434
Creator: U.S. Food and Drug Administration
Published: 2009-07-06

Substantially Equivalent

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

FDA 510(k) clearance K090434 for BECE PRESS, Substantially Equivalent on 2009-07-06. Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. Device class: 2.

Clearance details

Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2009-02-19
Decision date: 2009-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bremen, DE

Download summary PDF View on FDA.gov ↗

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