Exciplex— 510(k) K191086

Substantially Equivalent

Clarteis

FDA 510(k) clearance K191086 for Exciplex, Substantially Equivalent on 2019-12-11. Applicant: Clarteis. Device class: 2.

Clearance details

Applicant: Clarteis
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 2019-04-24
Decision date: 2019-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valbonne, 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.