ANTERIORS AND POSTERIORS, PLASTIC— 510(k) K780217

Name: FDA 510(k) clearance K780217
Creator: U.S. Food and Drug Administration
Published: 1978-03-15

Substantially Equivalent

Dentsply Intl.

FDA 510(k) clearance K780217 for ANTERIORS AND POSTERIORS, PLASTIC, Substantially Equivalent on 1978-03-15. Applicant: Dentsply Intl.. Device class: 2.

Clearance details

Applicant: Dentsply Intl.
Product code: Code ELM
Device class: Class 2
Regulation: 21 CFR 872.3590
Advisory panel: Dental
Date received: 1978-02-10
Decision date: 1978-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.