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FDA 510(k), K202243, SkinPen Precision System
FDA 510(k), K202243, SkinPen Precision System
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$149.00 USD
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510(K) Number: K202243
Device Name: SkinPen Precision System
Manufacturer: Crown Aesthetics
Device Classification Name: powered microneedle device
Regulation Number: 878.4430
Classification Product Code: QAI
Date Received: 08/10/2020
Decision Date: 04/02/2021
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SkinPen Precision System
Manufacturer: Crown Aesthetics
Device Classification Name: powered microneedle device
Regulation Number: 878.4430
Classification Product Code: QAI
Date Received: 08/10/2020
Decision Date: 04/02/2021
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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