PIEZOTOME CUBE— 510(k) K172137

Substantially Equivalent

Satelec - Acteon Group

FDA 510(k) clearance K172137 for PIEZOTOME CUBE, Substantially Equivalent on 2018-05-03. Applicant: Satelec - Acteon Group. Device class: 2.

Clearance details

Applicant: Satelec - Acteon Group
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2017-07-17
Decision date: 2018-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Merignac, FR

Download summary PDF View on FDA.gov ↗

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