VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40— 510(k) K052130

Name: FDA 510(k) clearance K052130
Creator: U.S. Food and Drug Administration
Published: 2005-08-15

Substantially Equivalent

Vident

FDA 510(k) clearance K052130 for VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40, Substantially Equivalent on 2005-08-15. Applicant: Vident. Device class: 2.

Clearance details

Applicant: Vident
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2005-08-05
Decision date: 2005-08-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

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