MEISINGER BENEX, MODEL BE001— 510(k) K062130
Substantially EquivalentHager& Meisinger GmbH
FDA 510(k) clearance K062130 for MEISINGER BENEX, MODEL BE001, Substantially Equivalent on 2007-04-16. Applicant: Hager& Meisinger GmbH.
Clearance details
- Applicant
- Hager& Meisinger GmbH
- Product code
- Code EMG
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Centennial, CO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.