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FDA 510(k)

Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K

K-Number: K221569 · 2022-06-30

Decision Date2022-06-30
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K is a medical device manufactured by Shenzhen Fansizhe Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-30 under approval number K221569. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

Related Clinical Trials

Other Devices by Shenzhen Fansizhe Science and Technology Co., Ltd.

Related Devices (Code: OHT)

Official Source

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