Photodynamic Therapy (PDT) Equipment
K-Number: K200751 · 2020-05-21
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
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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.