ARTIFICIAL TEETH, PORCELAIN, MODIFIED— 510(k) K860608

Name: FDA 510(k) clearance K860608
Creator: U.S. Food and Drug Administration
Published: 1986-03-26

Substantially Equivalent

Dentsply Intl.

FDA 510(k) clearance K860608 for ARTIFICIAL TEETH, PORCELAIN, MODIFIED, Substantially Equivalent on 1986-03-26. Applicant: Dentsply Intl.. Device class: 2.

Clearance details

Applicant: Dentsply Intl.
Product code: Code ELL
Device class: Class 2
Regulation: 21 CFR 872.3920
Advisory panel: Dental
Date received: 1986-02-19
Decision date: 1986-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: York, PA, US

Download summary PDF View on FDA.gov ↗

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