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FDA 510(k)

Picosecond Nd:YAG Laser (PICOCAREMAJESTY)

K-Number: K241144 · 2024-06-24

Decision Date2024-06-24
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Picosecond Nd:YAG Laser (PICOCAREMAJESTY) is a medical device manufactured by Wontech Co., Ltd.. It received FDA 510(k) clearance on 2024-06-24 under approval number K241144. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Picosecond Nd:YAG Laser (PICOCAREMAJESTY)?

Picosecond Nd:YAG Laser (PICOCAREMAJESTY) is a medical device that received FDA 510(k) clearance on 2024-06-24. It is manufactured by Wontech Co., Ltd.. The 510(k) number is K241144.

When was Picosecond Nd:YAG Laser (PICOCAREMAJESTY) approved by the FDA?

Picosecond Nd:YAG Laser (PICOCAREMAJESTY) received FDA 510(k) clearance on 2024-06-24, under approval number K241144.

What company makes Picosecond Nd:YAG Laser (PICOCAREMAJESTY)?

Picosecond Nd:YAG Laser (PICOCAREMAJESTY) is manufactured by Wontech Co., Ltd..

What is the FDA product code for Picosecond Nd:YAG Laser (PICOCAREMAJESTY)?

The FDA product code for Picosecond Nd:YAG Laser (PICOCAREMAJESTY) is GEX. This falls under the Gastroenterology category.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.