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FDA 510(k)

Diode Laser Hair Removal System (SH-VD910)

Número K: K240520 · 2024-05-20

RequerenteBeijing Sea Heart International Science and Technologyco.Ltd
Data da decisão2024-05-20
Código do produtoGEX
Comité consultivoSU
DecisãoSubstantially Equivalent

Resumo do dispositivo

Diode Laser Hair Removal System (SH-VD910) is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Sea Heart International Science and Technologyco.Ltd. It received FDA 510(k) clearance on 2024-05-20 under 510(k) number K240520. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Diode Laser Hair Removal System (SH-VD910)?

Diode Laser Hair Removal System (SH-VD910) is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Beijing Sea Heart International Science and Technologyco.Ltd. The 510(k) number is K240520.

When did Diode Laser Hair Removal System (SH-VD910) receive FDA 510(k) clearance?

Diode Laser Hair Removal System (SH-VD910) received FDA 510(k) clearance on 2024-05-20, under 510(k) number K240520.

Who is the listed applicant for Diode Laser Hair Removal System (SH-VD910)?

The FDA 510(k) record lists Beijing Sea Heart International Science and Technologyco.Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Diode Laser Hair Removal System (SH-VD910)?

The FDA product code for Diode Laser Hair Removal System (SH-VD910) is GEX. This falls under the Gastroenterology category.

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Fonte oficial

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