DENTATUS OSCIOMAT— 510(k) K031793

Substantially Equivalent

Dentatus USA , Ltd.

FDA 510(k) clearance K031793 for DENTATUS OSCIOMAT, Substantially Equivalent on 2003-11-13. Applicant: Dentatus USA , Ltd.. Device class: 2.

Clearance details

Applicant: Dentatus USA , Ltd.
Product code: Code DZH
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2003-06-10
Decision date: 2003-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sound Beach, NY, US

Download summary PDF View on FDA.gov ↗

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