MODIFICATION TO:REGISTRADO X-TRA— 510(k) K051535

Substantially Equivalent

Voco 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: Product code ELW
Device class: Class 2
Regulation: 21 CFR 872.3660
Advisory panel: Dental
Date received: 2005-06-10
Decision date: 2005-06-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Bend, OR, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.