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FDA 510(k)

IPL Hair Removal Device Joy Version

K-Number: K173813 · 2018-09-07

Decision Date2018-09-07
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device Joy Version is the device name listed in this FDA 510(k) record. The listed applicant is Shen Zhen Cosbeauty Co., Ltd.. It received FDA 510(k) clearance on 2018-09-07 under 510(k) 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. The listed applicant is Shen Zhen Cosbeauty Co., Ltd.. The 510(k) number is K173813.

When did IPL Hair Removal Device Joy Version receive FDA 510(k) clearance?

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

Who is the listed applicant for IPL Hair Removal Device Joy Version?

The FDA 510(k) record lists Shen Zhen Cosbeauty Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Shen Zhen Cosbeauty Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: OHT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.