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FDA 510(k)

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)

K-Number: K251000 · 2025-06-30

ApplicantShenzhen Chuangtong Yigou Technology Co., Ltd.
Decision Date2025-06-30
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is a medical device manufactured by Shenzhen Chuangtong Yigou Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-06-30 under approval number K251000. 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 Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is a medical device that received FDA 510(k) clearance on 2025-06-30. It is manufactured by Shenzhen Chuangtong Yigou Technology Co., Ltd.. The 510(k) number is K251000.

When was Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) approved by the FDA?

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) received FDA 510(k) clearance on 2025-06-30, under approval number K251000.

What company makes Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is manufactured by Shenzhen Chuangtong Yigou Technology Co., Ltd..

What is the FDA product code for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?

The FDA product code for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) is OHT.

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Other Devices by Shenzhen Chuangtong Yigou Technology Co., Ltd.

K254047Hair Removal Device (CT10, CT10 Pro, CT11, CT11 Pro, CT12, CT12 Pro, CTU05, CTU07, CTU09, CTU012, CTU015, CTU X, DT015 Pro, DT015, DT017 Pro, DT017, DT025 Pro, DT025)

Related Devices (Code: 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.

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