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FDA 510(k)

IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32

K-Number: K230021 · 2023-03-31

Decision Date2023-03-31
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 is a medical device manufactured by Shenzhen Yangyi Technology ., Ltd.. It received FDA 510(k) clearance on 2023-03-31 under approval number K230021. 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, Model(s): AP10, AP20, AP30, AP32?

IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 is a medical device that received FDA 510(k) clearance on 2023-03-31. It is manufactured by Shenzhen Yangyi Technology ., Ltd.. The 510(k) number is K230021.

When was IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 approved by the FDA?

IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 received FDA 510(k) clearance on 2023-03-31, under approval number K230021.

What company makes IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32?

IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 is manufactured by Shenzhen Yangyi Technology ., Ltd..

What is the FDA product code for IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32?

The FDA product code for IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32 is OHT.

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