Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)
K-Number: K251000 · 2025-06-30
Device Summary
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. The listed applicant is Shenzhen Chuangtong Yigou Technology Co., Ltd.. The 510(k) number is K251000.
When did Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) receive FDA 510(k) clearance?
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 510(k) number K251000.
Who is the listed applicant for Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)?
The FDA 510(k) record lists Shenzhen Chuangtong Yigou Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Shenzhen Chuangtong Yigou Technology 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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