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FDA 510(k)

Medi Lift PLUS

K-Number: K220198 · 2023-06-28

ApplicantYa-Man, Ltd.
Decision Date2023-06-28
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Medi Lift PLUS is a medical device manufactured by Ya-Man, Ltd.. It received FDA 510(k) clearance on 2023-06-28 under approval number K220198. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medi Lift PLUS?

Medi Lift PLUS is a medical device that received FDA 510(k) clearance on 2023-06-28. It is manufactured by Ya-Man, Ltd.. The 510(k) number is K220198.

When was Medi Lift PLUS approved by the FDA?

Medi Lift PLUS received FDA 510(k) clearance on 2023-06-28, under approval number K220198.

What company makes Medi Lift PLUS?

Medi Lift PLUS is manufactured by Ya-Man, Ltd..

What is the FDA product code for Medi Lift PLUS?

The FDA product code for Medi Lift PLUS is NFO.

Other Devices by Ya-Man, Ltd.

K250618Medi Lift Essential Eye Mask K244048Medi Lift Mask

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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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