RDT3 HANDPIECE HEAD MODEL RDT3— 510(k) K101172

Name: FDA 510(k) clearance K101172
Creator: U.S. Food and Drug Administration
Published: 2010-07-27

Substantially Equivalent

Redent Nova, Ltd.

FDA 510(k) clearance K101172 for RDT3 HANDPIECE HEAD MODEL RDT3, Substantially Equivalent on 2010-07-27. Applicant: Redent Nova, Ltd.. Device class: 1.

Clearance details

Applicant: Redent Nova, Ltd.
Product code: Code EFA
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2010-04-26
Decision date: 2010-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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