DIAGNODENT— 510(k) K051909
Substantially EquivalentKavo America
FDA 510(k) clearance K051909 for DIAGNODENT, Substantially Equivalent on 2005-10-21. Applicant: Kavo America. Device class: 2.
Clearance details
- Applicant
- Kavo America
- Product code
- Code NBL
- Device class
- Class 2
- Regulation
- 21 CFR 872.1745
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Deer Field, IL, US
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