REMIN PRO— 510(k) K101104

Substantially Equivalent

Voco GmbH

FDA 510(k) clearance K101104 for REMIN PRO, Substantially Equivalent on 2010-10-21. Applicant: Voco GmbH. Device class: 1.

Clearance details

Applicant: Voco GmbH
Product code: Code EJR
Device class: Class 1
Regulation: 21 CFR 872.6030
Advisory panel: Dental
Date received: 2010-04-20
Decision date: 2010-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cuxhaven, DE

Download summary PDF View on FDA.gov ↗

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