Hair Removal Device, Model(s): R2815-G Pro, R2815-G
K-Number: K232575 · 2023-11-20
Decision Date2023-11-20
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Hair Removal Device, Model(s): R2815-G Pro, R2815-G is a medical device manufactured by Shenzhen Jianchao Intelligent Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-11-20 under approval number K232575. 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(s): R2815-G Pro, R2815-G?
Hair Removal Device, Model(s): R2815-G Pro, R2815-G is a medical device that received FDA 510(k) clearance on 2023-11-20. It is manufactured by Shenzhen Jianchao Intelligent Technology Co., Ltd.. The 510(k) number is K232575.
When was Hair Removal Device, Model(s): R2815-G Pro, R2815-G approved by the FDA?
Hair Removal Device, Model(s): R2815-G Pro, R2815-G received FDA 510(k) clearance on 2023-11-20, under approval number K232575.
What company makes Hair Removal Device, Model(s): R2815-G Pro, R2815-G?
Hair Removal Device, Model(s): R2815-G Pro, R2815-G is manufactured by Shenzhen Jianchao Intelligent Technology Co., Ltd..
What is the FDA product code for Hair Removal Device, Model(s): R2815-G Pro, R2815-G?
The FDA product code for Hair Removal Device, Model(s): R2815-G Pro, R2815-G is OHT.
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Other Devices by Shenzhen Jianchao Intelligent Technology Co., Ltd.
K242710Hair Removal Device (R3C16-P, R3C16-W, R3C16-G, R3C16-P Pro, R3C16-W Pro, R3C16-G Pro, R3505-W, R3505-B, R3505-W Pro, R3505-B Pro)
K252553Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)
K253833Facial & Body Beauty Device (model: INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)
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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.