IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9
K-Number: K231800 · 2023-09-07
ApplicantShenzhen Qianyu Technology Co., Ltd.
Decision Date2023-09-07
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 is a medical device manufactured by Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-09-07 under approval number K231800. 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): JP1, JR3, JR8, JR9?
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 is a medical device that received FDA 510(k) clearance on 2023-09-07. It is manufactured by Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K231800.
When was IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 approved by the FDA?
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 received FDA 510(k) clearance on 2023-09-07, under approval number K231800.
What company makes IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9?
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 is manufactured by Shenzhen Qianyu Technology Co., Ltd..
What is the FDA product code for IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9?
The FDA product code for IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 is OHT.
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Official Source
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