VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY— 510(k) K932893

Name: FDA 510(k) clearance K932893
Creator: U.S. Food and Drug Administration
Published: 1994-03-28

Substantially Equivalent

Vident

FDA 510(k) clearance K932893 for VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY, Substantially Equivalent on 1994-03-28. Applicant: Vident. Device class: 2.

Clearance details

Applicant: Vident
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 1993-06-10
Decision date: 1994-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldwin Park, CA, US

Download summary PDF View on FDA.gov ↗

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