PREMIER INLAY PLACER— 510(k) K781034

Name: FDA 510(k) clearance K781034
Creator: U.S. Food and Drug Administration
Published: 1978-06-30

Substantially Equivalent

Premier Dental Products Co.

FDA 510(k) clearance K781034 for PREMIER INLAY PLACER, Substantially Equivalent on 1978-06-30. Applicant: Premier Dental Products Co.. Device class: 1.

Clearance details

Applicant: Premier Dental Products Co.
Product code: Code EKI
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1978-06-19
Decision date: 1978-06-30
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.