BEGOPAL+— 510(k) K123929

Name: FDA 510(k) clearance K123929
Creator: U.S. Food and Drug Administration
Published: 2013-03-14

Substantially Equivalent

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

FDA 510(k) clearance K123929 for BEGOPAL+, Substantially Equivalent on 2013-03-14. Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. Device class: 2.

Clearance details

Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 2012-12-20
Decision date: 2013-03-14
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Bremen, DE

Download summary PDF View on FDA.gov ↗

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