Cervitec F— 510(k) K191453
Substantially EquivalentIvoclar Vivadent, AG
FDA 510(k) clearance K191453 for Cervitec F, Substantially Equivalent on 2020-02-11. Applicant: Ivoclar Vivadent, AG. Device class: 2.
Clearance details
- Applicant
- Ivoclar Vivadent, AG
- Product code
- Code LBH
- Device class
- Class 2
- Regulation
- 21 CFR 872.3260
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Schaan, LI
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