Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LipiVage

K-Number: K172714 · 2017-12-08

ApplicantGenesis Biosystems, Inc.
Decision Date2017-12-08
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LipiVage is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Biosystems, Inc.. It received FDA 510(k) clearance on 2017-12-08 under 510(k) number K172714. 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 LipiVage?

LipiVage is a medical device that received FDA 510(k) clearance on 2017-12-08. The listed applicant is Genesis Biosystems, Inc.. The 510(k) number is K172714.

When did LipiVage receive FDA 510(k) clearance?

LipiVage received FDA 510(k) clearance on 2017-12-08, under 510(k) number K172714.

Who is the listed applicant for LipiVage?

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

What is the FDA product code for LipiVage?

The FDA product code for LipiVage is MUU.

Related Devices (Code: MUU)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) KitMillennium Medical Technologies Inc (Dba Cellmyx)K203800SyntrFuge SystemSyntr Health Technologies, Inc.K202443Smart Kit Basic, Smart Kit ProBsl Co., Ltd.K193539REVOLVE ENVI 600 Advanced Adipose SystemLifecell CorporationK193363Dermapose RefreshPuregraft, LLCK182732JTL-250-01Jointechlabs, Inc.

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.

↑