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FDA 510(k)

IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)

K-Number: K232499 · 2023-10-11

Decision Date2023-10-11
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device (LS-T106, LS-T107, LS-T108) is a medical device manufactured by Shenzhen Lescolton Electrical Appliance Co., Ltd.. It received FDA 510(k) clearance on 2023-10-11 under approval number K232499. 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 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 →

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