Picosecond Nd:YAG Laser (PICOCAREMAJESTY)
K-Number: K241144 · 2024-06-24
Device Summary
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.
Other Devices by Wontech Co., Ltd.
Related Devices (Code: GEX)
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.