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FDA 510(k)

IPL Hair Removal Device Joy Version

K-Number: K173813 · 2018-09-07

ApplicantShen Zhen Cosbeauty Co., Ltd.
Decision Date2018-09-07
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device Joy Version is a medical device manufactured by Shen Zhen Cosbeauty Co., Ltd.. It received FDA 510(k) clearance on 2018-09-07 under approval number K173813. 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 Joy Version?

IPL Hair Removal Device Joy Version is a medical device that received FDA 510(k) clearance on 2018-09-07. It is manufactured by Shen Zhen Cosbeauty Co., Ltd.. The 510(k) number is K173813.

When was IPL Hair Removal Device Joy Version approved by the FDA?

IPL Hair Removal Device Joy Version received FDA 510(k) clearance on 2018-09-07, under approval number K173813.

What company makes IPL Hair Removal Device Joy Version?

IPL Hair Removal Device Joy Version is manufactured by Shen Zhen Cosbeauty Co., Ltd..

What is the FDA product code for IPL Hair Removal Device Joy Version?

The FDA product code for IPL Hair Removal Device Joy Version is OHT.

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Related PubMed Literature

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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.

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