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FDA 510(k)

Nd: YAG Laser Therapy System (QN-1)

K-Number: K250722 · 2025-06-06

Decision Date2025-06-06
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Nd: YAG Laser Therapy System (QN-1) is a medical device manufactured by Hebei JT Medical Co., Ltd.. It received FDA 510(k) clearance on 2025-06-06 under approval number K250722. 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 Nd: YAG Laser Therapy System (QN-1)?

Nd: YAG Laser Therapy System (QN-1) is a medical device that received FDA 510(k) clearance on 2025-06-06. It is manufactured by Hebei JT Medical Co., Ltd.. The 510(k) number is K250722.

When was Nd: YAG Laser Therapy System (QN-1) approved by the FDA?

Nd: YAG Laser Therapy System (QN-1) received FDA 510(k) clearance on 2025-06-06, under approval number K250722.

What company makes Nd: YAG Laser Therapy System (QN-1)?

Nd: YAG Laser Therapy System (QN-1) is manufactured by Hebei JT Medical Co., Ltd..

What is the FDA product code for Nd: YAG Laser Therapy System (QN-1)?

The FDA product code for Nd: YAG Laser Therapy System (QN-1) is GEX. This falls under the Gastroenterology category.

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Official Source

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