FDA 510(k)

Massager de Perna de Compressão de Ar (Modelos: S9036C, S9036B e S9036A)

Número K: K222206 · 2022-09-30

RequerenteShenzhen Dongjilian Medical Tech Co., Ltd.

Data da decisão2022-09-30

Código do produtoIRP

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do dispositivo

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongjilian Medical Tech Co., Ltd.. It received FDA 510(k) clearance on 2022-09-30 under 510(k) number K222206. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is a medical device that received FDA 510(k) clearance on 2022-09-30. The listed applicant is Shenzhen Dongjilian Medical Tech Co., Ltd.. The 510(k) number is K222206.

When did Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) receive FDA 510(k) clearance?

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) received FDA 510(k) clearance on 2022-09-30, under 510(k) number K222206.

Who is the listed applicant for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?

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

What is the FDA product code for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?

The FDA product code for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is IRP.

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Outros registros que listam Shenzhen Dongjilian Medical Tech Co., Ltd. como candidato(a)

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Fonte oficial

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