ULTHERA SYSTEM, MODEL 8850-0001— 510(k) DEN080006

Unknown

Ulthera, Inc.

FDA 510(k) clearance DEN080006 for ULTHERA SYSTEM, MODEL 8850-0001, Unknown on 2009-09-11. Applicant: Ulthera, Inc.. Device class: 2.

Clearance details

Applicant: Ulthera, Inc.
Product code: Code OHV
Device class: Class 2
Regulation: 21 CFR 878.4590
Advisory panel: General, Plastic Surgery
Date received: 2008-04-11
Decision date: 2009-09-11
Decision: Unknown
Clearance type: Post-NSE
Location: Mesa, AZ, US

View on FDA.gov ↗

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