Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K
K-Number: K221569 · 2022-06-30
Device Summary
Frequently Asked Questions
What is the Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K?
Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K is a medical device that received FDA 510(k) clearance on 2022-06-30. It is manufactured by Shenzhen Fansizhe Science and Technology Co., Ltd.. The 510(k) number is K221569.
When was Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K approved by the FDA?
Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K received FDA 510(k) clearance on 2022-06-30, under approval number K221569.
What company makes Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K?
Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K is manufactured by Shenzhen Fansizhe Science and Technology Co., Ltd..
What is the FDA product code for Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K?
The FDA product code for Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K is OHT.
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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.