CERAPALL 6 -- MODIFIED— 510(k) K924292

Name: FDA 510(k) clearance K924292
Creator: U.S. Food and Drug Administration
Published: 1993-03-01

Substantially Equivalent

Metalor Dental USA Corp.

FDA 510(k) clearance K924292 for CERAPALL 6 -- MODIFIED, Substantially Equivalent on 1993-03-01. Applicant: Metalor Dental USA Corp.. Device class: 2.

Clearance details

Applicant: Metalor Dental USA Corp.
Product code: Code EJS
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 1992-06-29
Decision date: 1993-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville Centre, NY, US

Download summary PDF View on FDA.gov ↗

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