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FDA 510(k), K161636, Lipogems System
FDA 510(k), K161636, Lipogems System
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510(K) Number: K161636
Device Name: Lipogems System
Manufacturer: Lipogems International SpA
Device Classification Name: System, Suction, Lipoplasty
Regulation Number: 878.5040
Classification Product Code: MUU
Date Received: 06/14/2016
Decision Date: 11/04/2016
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Lipogems System
Manufacturer: Lipogems International SpA
Device Classification Name: System, Suction, Lipoplasty
Regulation Number: 878.5040
Classification Product Code: MUU
Date Received: 06/14/2016
Decision Date: 11/04/2016
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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