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FDA 510(k)

Liposaver

K-Number: K212969 · 2024-08-07

ApplicantLhbiomed Co., Ltd.
Decision Date2024-08-07
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Liposaver is a medical device manufactured by Lhbiomed Co., Ltd.. It received FDA 510(k) clearance on 2024-08-07 under approval number K212969. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Liposaver?

Liposaver is a medical device that received FDA 510(k) clearance on 2024-08-07. It is manufactured by Lhbiomed Co., Ltd.. The 510(k) number is K212969.

When was Liposaver approved by the FDA?

Liposaver received FDA 510(k) clearance on 2024-08-07, under approval number K212969.

What company makes Liposaver?

Liposaver is manufactured by Lhbiomed Co., Ltd..

What is the FDA product code for Liposaver?

The FDA product code for Liposaver is QPB.

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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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