FDA 510(k)

Intense Pulse Light Therapeutic Apparatus

Número K: K232932 · 2023-12-04

RequerenteShenzhen Greatro Electronic Technology Co., Ltd.

Data da decisão2023-12-04

Código do produtoOHT

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Intense Pulse Light Therapeutic Apparatus is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Greatro Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-04 under 510(k) number K232932. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Intense Pulse Light Therapeutic Apparatus?

Intense Pulse Light Therapeutic Apparatus is a medical device that received FDA 510(k) clearance on 2023-12-04. The listed applicant is Shenzhen Greatro Electronic Technology Co., Ltd.. The 510(k) number is K232932.

When did Intense Pulse Light Therapeutic Apparatus receive FDA 510(k) clearance?

Intense Pulse Light Therapeutic Apparatus received FDA 510(k) clearance on 2023-12-04, under 510(k) number K232932.

Who is the listed applicant for Intense Pulse Light Therapeutic Apparatus?

The FDA 510(k) record lists Shenzhen Greatro Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intense Pulse Light Therapeutic Apparatus?

The FDA product code for Intense Pulse Light Therapeutic Apparatus is OHT.

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Outros registros que listam Shenzhen Greatro Electronic Technology Co., Ltd. como candidato(a)

K242595Intense Pulse Light Therapeutic Apparatus (IPL-18 BF, IPL-18 FG)

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