VITA CAD-TEMP FOR INLAB, MODEL, VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310— 510(k) K070991

Name: FDA 510(k) clearance K070991
Creator: U.S. Food and Drug Administration
Published: 2007-06-01

Substantially Equivalent

Vita

FDA 510(k) clearance K070991 for VITA CAD-TEMP FOR INLAB, MODEL, VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310, Substantially Equivalent on 2007-06-01. Applicant: Vita. Device class: 2.

Clearance details

Applicant: Vita
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2007-04-09
Decision date: 2007-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, 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.