PREVI DENT PROPHYLAXIS MINT NDC— 510(k) K780834

Name: FDA 510(k) clearance K780834
Creator: U.S. Food and Drug Administration
Published: 1978-06-02

Substantially Equivalent

Hoyt Laboratories

FDA 510(k) clearance K780834 for PREVI DENT PROPHYLAXIS MINT NDC, Substantially Equivalent on 1978-06-02. Applicant: Hoyt Laboratories. Device class: 1.

Clearance details

Applicant: Hoyt Laboratories
Product code: Code EJR
Device class: Class 1
Regulation: 21 CFR 872.6030
Advisory panel: Dental
Date received: 1978-05-24
Decision date: 1978-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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