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FDA 510(k), K171323, BIOPHOTAS CELLUMA3
FDA 510(k), K171323, BIOPHOTAS CELLUMA3
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510(K) Number: K171323
Device Name: BIOPHOTAS CELLUMA3
Manufacturer: Biophotas Inc
Device Classification Name: light based over the counter wrinkle reduction
Regulation Number: 878.4810
Classification Product Code: OHS
Date Received: 05/05/2017
Decision Date: 09/01/2017
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BIOPHOTAS CELLUMA3
Manufacturer: Biophotas Inc
Device Classification Name: light based over the counter wrinkle reduction
Regulation Number: 878.4810
Classification Product Code: OHS
Date Received: 05/05/2017
Decision Date: 09/01/2017
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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