CAVIOS CAVITY LINER— 510(k) K111668

Name: FDA 510(k) clearance K111668
Creator: U.S. Food and Drug Administration
Published: 2011-08-19

Substantially Equivalent

Neodental Chemical Products Co., Ltd.

FDA 510(k) clearance K111668 for CAVIOS CAVITY LINER, Substantially Equivalent on 2011-08-19. Applicant: Neodental Chemical Products Co., Ltd.. Device class: 2.

Clearance details

Applicant: Neodental Chemical Products Co., Ltd.
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 2011-06-14
Decision date: 2011-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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