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FDA 510(k)

Nd: YAG Laser Therapy Systems

K-Number: K193477 · 2020-06-24

Decision Date2020-06-24
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Nd: YAG Laser Therapy Systems is a medical device manufactured by Beijing Kes Biology Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-06-24 under approval number K193477. 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 Systems?

Nd: YAG Laser Therapy Systems is a medical device that received FDA 510(k) clearance on 2020-06-24. It is manufactured by Beijing Kes Biology Technology Co., Ltd.. The 510(k) number is K193477.

When was Nd: YAG Laser Therapy Systems approved by the FDA?

Nd: YAG Laser Therapy Systems received FDA 510(k) clearance on 2020-06-24, under approval number K193477.

What company makes Nd: YAG Laser Therapy Systems?

Nd: YAG Laser Therapy Systems is manufactured by Beijing Kes Biology Technology Co., Ltd..

What is the FDA product code for Nd: YAG Laser Therapy Systems?

The FDA product code for Nd: YAG Laser Therapy Systems is GEX. This falls under the Gastroenterology category.

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Official Source

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