FDA 510(k)

Electric wheelchair (S7018)

Número K: K240270 · 2024-08-27

RequerenteGuangdong Prestige Technology Company Limited

Data da decisão2024-08-27

Código do produtoITI

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electric wheelchair (S7018) is the device name listed in this FDA 510(k) record. The listed applicant is Guangdong Prestige Technology Company Limited. It received FDA 510(k) clearance on 2024-08-27 under 510(k) number K240270. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electric wheelchair (S7018)?

Electric wheelchair (S7018) is a medical device that received FDA 510(k) clearance on 2024-08-27. The listed applicant is Guangdong Prestige Technology Company Limited. The 510(k) number is K240270.

When did Electric wheelchair (S7018) receive FDA 510(k) clearance?

Electric wheelchair (S7018) received FDA 510(k) clearance on 2024-08-27, under 510(k) number K240270.

Who is the listed applicant for Electric wheelchair (S7018)?

The FDA 510(k) record lists Guangdong Prestige Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electric wheelchair (S7018)?

The FDA product code for Electric wheelchair (S7018) is ITI.

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