W&H HANDPIECE ANESTO, MODEL: RA-5— 510(k) K083811
Substantially EquivalentW&H Dentalwerk Buermoos GmbH
FDA 510(k) clearance K083811 for W&H HANDPIECE ANESTO, MODEL: RA-5, Substantially Equivalent on 2010-01-14. Applicant: W&H Dentalwerk Buermoos GmbH. Device class: 2.
Clearance details
- Applicant
- W&H Dentalwerk Buermoos GmbH
- Product code
- Code EGM
- Device class
- Class 2
- Regulation
- 21 CFR 872.4475
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Buermoos, AT
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Data sourced from openFDA. This site is unofficial and independent of the FDA.