IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002
K-Number: K232056 · 2023-10-06
Device Summary
Frequently Asked Questions
What is the IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002?
IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002 is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Dongguan Lide Electric Appliance Co., Ltd.. The 510(k) number is K232056.
When did IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002 receive FDA 510(k) clearance?
IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002 received FDA 510(k) clearance on 2023-10-06, under 510(k) number K232056.
Who is the listed applicant for IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002?
The FDA 510(k) record lists Dongguan Lide Electric Appliance 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): PB1, PB2, PB3, PB4, TM002?
The FDA product code for IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002 is OHT.
Other records listing Dongguan Lide Electric Appliance 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.