Ceramir Restore QuikCap— 510(k) K201937
Substantially EquivalentDoxa Dental AB
FDA 510(k) clearance K201937 for Ceramir Restore QuikCap, Substantially Equivalent on 2020-11-13. Applicant: Doxa Dental AB. Device class: 2.
Clearance details
- Applicant
- Doxa Dental AB
- Product code
- Code EMA
- Device class
- Class 2
- Regulation
- 21 CFR 872.3275
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Uppsala, SE
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