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FDA 510(k)

LYMA Laser

K-Number: K210823 · 2022-03-18

ApplicantLyma Life , Ltd.
Decision Date2022-03-18
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LYMA Laser is a medical device manufactured by Lyma Life , Ltd.. It received FDA 510(k) clearance on 2022-03-18 under approval number K210823. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYMA Laser?

LYMA Laser is a medical device that received FDA 510(k) clearance on 2022-03-18. It is manufactured by Lyma Life , Ltd.. The 510(k) number is K210823.

When was LYMA Laser approved by the FDA?

LYMA Laser received FDA 510(k) clearance on 2022-03-18, under approval number K210823.

What company makes LYMA Laser?

LYMA Laser is manufactured by Lyma Life , Ltd..

What is the FDA product code for LYMA Laser?

The FDA product code for LYMA Laser is OHS.

Other Devices by Lyma Life , Ltd.

K243330LYMA Laser PRO

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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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