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FDA 510(k), K120737, TRIA LASER HAIR REMOVAL SYSTEM
FDA 510(k), K120737, TRIA LASER HAIR REMOVAL SYSTEM
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510(K) Number: K120737
Device Name: TRIA LASER HAIR REMOVAL SYSTEM
Manufacturer: TRIA BEAUTY, INC.
Device Classification Name: powered laser surgical instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 03/09/2012
Decision Date: 09/13/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TRIA LASER HAIR REMOVAL SYSTEM
Manufacturer: TRIA BEAUTY, INC.
Device Classification Name: powered laser surgical instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 03/09/2012
Decision Date: 09/13/2012
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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