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FDA 510(k)

Alma LipoFlow System

K-Number: K171242 · 2017-07-14

ApplicantAlma Lasers, Inc.
Decision Date2017-07-14
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Alma LipoFlow System is a medical device manufactured by Alma Lasers, Inc.. It received FDA 510(k) clearance on 2017-07-14 under approval number K171242. 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 Alma LipoFlow System?

Alma LipoFlow System is a medical device that received FDA 510(k) clearance on 2017-07-14. It is manufactured by Alma Lasers, Inc.. The 510(k) number is K171242.

When was Alma LipoFlow System approved by the FDA?

Alma LipoFlow System received FDA 510(k) clearance on 2017-07-14, under approval number K171242.

What company makes Alma LipoFlow System?

Alma LipoFlow System is manufactured by Alma Lasers, Inc..

What is the FDA product code for Alma LipoFlow System?

The FDA product code for Alma LipoFlow System is MUU.

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Official Source

View on FDA Database →

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

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