FDA 510(k)

Lipogems System

K-Number: K171135 · 2017-05-18

Decision Date2017-05-18

Product CodeMUU

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Lipogems System is a medical device manufactured by Lipogems International Spa. It received FDA 510(k) clearance on 2017-05-18 under approval number K171135. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lipogems System?

Lipogems System is a medical device that received FDA 510(k) clearance on 2017-05-18. It is manufactured by Lipogems International Spa. The 510(k) number is K171135.

When was Lipogems System approved by the FDA?

Lipogems System received FDA 510(k) clearance on 2017-05-18, under approval number K171135.

What company makes Lipogems System?

Lipogems System is manufactured by Lipogems International Spa.

What is the FDA product code for Lipogems System?

The FDA product code for Lipogems System is MUU.

Other Devices by Lipogems International Spa

K161636Lipogems System

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K161636Lipogems SystemLipogems International Spa K172714LipiVageGenesis Biosystems, Inc. K163647Revolve Envi 600 Advanced Adipose SystemLifecell Corporation K171242Alma LipoFlow SystemAlma Lasers, Inc. K170449Autoclavable Suction Jar with Luer Lock extension - 250, 500, 1,000, 2,000 and 3,000 ml, Autoclavable Suction Jar without Luer Lock extension - 1,500 and 2,500 ml, Sterile 1,500 and 2,500 Lids with Conical patient connection 6-10 and overflow protectionMillennium Medical Technologies, Inc. K161372The Red Head Collection Device, The Jordy Connection SystemMiami Fat Supply

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.