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. Device class: 2.

Clearance details

Applicant: Bellus Medical, LLC
Product code: Code QAI
Device class: Class 2
Regulation: 21 CFR 878.4430
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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Data sourced from openFDA. This site is unofficial and independent of the FDA.