ACRY PAN, VIPI DENT PLUS, BIOLUX, BIOLUX V, NEW DENT, DENTOLUXX, VIPI DENT N.H., VIPI DENT V— 510(k) K022300

Name: FDA 510(k) clearance K022300
Creator: U.S. Food and Drug Administration
Published: 2002-10-03

Substantially Equivalent

Dental Vipi Ltda

FDA 510(k) clearance K022300 for ACRY PAN, VIPI DENT PLUS, BIOLUX, BIOLUX V, NEW DENT, DENTOLUXX, VIPI DENT N.H., VIPI DENT V, Substantially Equivalent on 2002-10-03. Applicant: Dental Vipi Ltda. Device class: 2.

Clearance details

Applicant: Dental Vipi Ltda
Product code: Code ELM
Device class: Class 2
Regulation: 21 CFR 872.3590
Advisory panel: Dental
Date received: 2002-07-16
Decision date: 2002-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, CO, 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.