Ulthera System— 510(k) K180623

Substantially Equivalent

Ulthera, Inc.

FDA 510(k) clearance K180623 for Ulthera System, Substantially Equivalent on 2018-05-04. Applicant: Ulthera, Inc..

Clearance details

Applicant: Ulthera, Inc.
Product code: Code OHV
Advisory panel: General, Plastic Surgery
Date received: 2018-03-09
Decision date: 2018-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

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