IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)
K-Number: K232499 · 2023-10-11
Device Summary
Frequently Asked Questions
What is the IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)?
IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) is a medical device that received FDA 510(k) clearance on 2023-10-11. It is manufactured by Shenzhen Lescolton Electrical Appliance Co., Ltd.. The 510(k) number is K232499.
When was IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) approved by the FDA?
IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) received FDA 510(k) clearance on 2023-10-11, under approval number K232499.
What company makes IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)?
IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) is manufactured by Shenzhen Lescolton Electrical Appliance Co., Ltd..
What is the FDA product code for IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)?
The FDA product code for IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) is OHT.
Related Clinical Trials
Other Devices by Shenzhen Lescolton Electrical Appliance Co., Ltd.
Related Devices (Code: OHT)
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.