SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS— 510(k) K844349
Substantially EquivalentIvoclar USA, Inc.
FDA 510(k) clearance K844349 for SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS, Substantially Equivalent on 1984-12-03. 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
Recent devices under product code ELM
view allMore clearances from Ivoclar USA, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.