K-number	K212969
Device name	Liposaver
Applicant	Lhbiomed Co., Ltd.
Product code	QPB
Device class	Class II
Decision date	Aug 7, 2024
Decision	Substantially Equivalent
Regulation	878.5040

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Source

View the full FDA submission: accessdata.fda.gov

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Liposaver

Everything you need for a 510(k) submission. Nothing you don't.