SkinPen Precision System— 510(k) DEN160029

Unknown

Bellus Medical, LLC

FDA 510(k) clearance DEN160029 for SkinPen Precision System, Unknown on 2018-03-01. Applicant: Bellus Medical, LLC.

Clearance details

Applicant: Bellus Medical, LLC
Product code: Code QAI
Advisory panel: General, Plastic Surgery
Date received: 2016-07-05
Decision date: 2018-03-01
Decision: Unknown
Clearance type: Direct
Location: Dallas, TX, US

View on FDA.gov ↗

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