MEISINGER BENEX, MODEL BE001— 510(k) K062130

Name: FDA 510(k) clearance K062130
Creator: U.S. Food and Drug Administration
Published: 2007-04-16

Substantially Equivalent

Hager& Meisinger GmbH

FDA 510(k) clearance K062130 for MEISINGER BENEX, MODEL BE001, Substantially Equivalent on 2007-04-16. Applicant: Hager& Meisinger GmbH. Device class: 1.

Clearance details

Applicant: Hager& Meisinger GmbH
Product code: Code EMG
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 2006-07-26
Decision date: 2007-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Centennial, CO, US

Download summary PDF View on FDA.gov ↗

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