FDA 510(k)

DVT Motion Pneumatic Compression Device

Número K: K232270 · 2024-03-06

Data da decisão2024-03-06

Código do produtoJOW

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

DVT Motion Pneumatic Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Koge Micro Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under 510(k) number K232270. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the DVT Motion Pneumatic Compression Device?

DVT Motion Pneumatic Compression Device is a medical device that received FDA 510(k) clearance on 2024-03-06. The listed applicant is Koge Micro Tech Co., Ltd.. The 510(k) number is K232270.

When did DVT Motion Pneumatic Compression Device receive FDA 510(k) clearance?

DVT Motion Pneumatic Compression Device received FDA 510(k) clearance on 2024-03-06, under 510(k) number K232270.

Who is the listed applicant for DVT Motion Pneumatic Compression Device?

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

What is the FDA product code for DVT Motion Pneumatic Compression Device?

The FDA product code for DVT Motion Pneumatic Compression Device is JOW.

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