MODIFICATION TO:REGISTRADO X-TRA— 510(k) K051535
Substantially EquivalentVoco GmbH
FDA 510(k) clearance K051535 for MODIFICATION TO:REGISTRADO X-TRA, Substantially Equivalent on 2005-06-28. Applicant: Voco GmbH. Device class: 2.
Clearance details
- Applicant
- Voco GmbH
- Product code
- Code ELW
- Device class
- Class 2
- Regulation
- 21 CFR 872.3660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Bend, OR, US
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view allData sourced from openFDA. This site is unofficial and independent of the FDA.