SOPIX— 510(k) K142995

Substantially Equivalent

Sopro - Acteon Group

FDA 510(k) clearance K142995 for SOPIX, Substantially Equivalent on 2015-08-17. Applicant: Sopro - Acteon Group. Device class: 2.

Clearance details

Applicant: Sopro - Acteon Group
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2014-10-16
Decision date: 2015-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laciotat, FR

Download summary PDF View on FDA.gov ↗

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