Hair Removal Device (Model: IPL-D26, IPL-D19)
K-Number: K221643 · 2022-10-21
ApplicantShenzhen Desida Technology Co., Ltd.
Decision Date2022-10-21
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Hair Removal Device (Model: IPL-D26, IPL-D19) is a medical device manufactured by Shenzhen Desida Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-10-21 under approval number K221643. 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 Hair Removal Device (Model: IPL-D26, IPL-D19)?
Hair Removal Device (Model: IPL-D26, IPL-D19) is a medical device that received FDA 510(k) clearance on 2022-10-21. It is manufactured by Shenzhen Desida Technology Co., Ltd.. The 510(k) number is K221643.
When was Hair Removal Device (Model: IPL-D26, IPL-D19) approved by the FDA?
Hair Removal Device (Model: IPL-D26, IPL-D19) received FDA 510(k) clearance on 2022-10-21, under approval number K221643.
What company makes Hair Removal Device (Model: IPL-D26, IPL-D19)?
Hair Removal Device (Model: IPL-D26, IPL-D19) is manufactured by Shenzhen Desida Technology Co., Ltd..
What is the FDA product code for Hair Removal Device (Model: IPL-D26, IPL-D19)?
The FDA product code for Hair Removal Device (Model: IPL-D26, IPL-D19) is OHT.
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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.