IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG
K-Number: K230122 · 2023-04-10
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Device Summary
Frequently Asked Questions
What is the IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG?
IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG is a medical device that received FDA 510(k) clearance on 2023-04-10. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. The 510(k) number is K230122.
When did IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG receive FDA 510(k) clearance?
IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG received FDA 510(k) clearance on 2023-04-10, under 510(k) number K230122.
Who is the listed applicant for IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG?
The FDA 510(k) record lists Shenzhen Ulike Smart Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG?
The FDA product code for IPL Hair Removal Device, Model(s): UI04 SD, UI04 DG is OHT.
Related Clinical Trials
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.
Other records listing Shenzhen Ulike Smart Electronics 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
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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