SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH— 510(k) K864707
Substantially EquivalentIvoclar USA, Inc.
FDA 510(k) clearance K864707 for SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH, Substantially Equivalent on 1987-02-10. Applicant: Ivoclar USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Ivoclar USA, Inc.
- Product code
- Code ELM
- Device class
- Class 2
- Regulation
- 21 CFR 872.3590
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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