CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL)— 510(k) K973919

Name: FDA 510(k) clearance K973919
Creator: U.S. Food and Drug Administration
Published: 1997-12-16

Substantially Equivalent

Medental Intl.

FDA 510(k) clearance K973919 for CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL), Substantially Equivalent on 1997-12-16. Applicant: Medental Intl.. Device class: 2.

Clearance details

Applicant: Medental Intl.
Product code: Code LBH
Device class: Class 2
Regulation: 21 CFR 872.3260
Advisory panel: Dental
Date received: 1997-10-15
Decision date: 1997-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Evergreen, CO, US

Download summary PDF View on FDA.gov ↗

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