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FDA 510(k)

Photodynamic Therapy (PDT) Equipment

K-Number: K200751 · 2020-05-21

Decision Date2020-05-21
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Photodynamic Therapy (PDT) Equipment is a medical device manufactured by Shangdong Huamei Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-05-21 under approval number K200751. 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 Photodynamic Therapy (PDT) Equipment?

Photodynamic Therapy (PDT) Equipment is a medical device that received FDA 510(k) clearance on 2020-05-21. It is manufactured by Shangdong Huamei Technology Co., Ltd.. The 510(k) number is K200751.

When was Photodynamic Therapy (PDT) Equipment approved by the FDA?

Photodynamic Therapy (PDT) Equipment received FDA 510(k) clearance on 2020-05-21, under approval number K200751.

What company makes Photodynamic Therapy (PDT) Equipment?

Photodynamic Therapy (PDT) Equipment is manufactured by Shangdong Huamei Technology Co., Ltd..

What is the FDA product code for Photodynamic Therapy (PDT) Equipment?

The FDA product code for Photodynamic Therapy (PDT) Equipment is GEX. This falls under the Gastroenterology category.

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Official Source

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