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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 the device name listed in this FDA 510(k) record. The listed applicant is Alma Lasers, Inc.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) 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. The listed applicant is Alma Lasers, Inc.. The 510(k) number is K171242.

When did Alma LipoFlow System receive FDA 510(k) clearance?

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

Who is the listed applicant for Alma LipoFlow System?

The FDA 510(k) record lists Alma Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alma LipoFlow System?

The FDA product code for Alma LipoFlow System is MUU.

Other records listing Alma Lasers, Inc. as applicant

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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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