FDA 510(k)

VesoFlow Lite DVT Compression Device

Número K: K181217 · 2018-08-05

Data da decisão2018-08-05

Código do produtoJOW

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

VesoFlow Lite DVT Compression Device is the device name listed in this FDA 510(k) record. The listed applicant is Caremed Supply, Inc.. It received FDA 510(k) clearance on 2018-08-05 under 510(k) number K181217. 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 VesoFlow Lite DVT Compression Device?

VesoFlow Lite DVT Compression Device is a medical device that received FDA 510(k) clearance on 2018-08-05. The listed applicant is Caremed Supply, Inc.. The 510(k) number is K181217.

When did VesoFlow Lite DVT Compression Device receive FDA 510(k) clearance?

VesoFlow Lite DVT Compression Device received FDA 510(k) clearance on 2018-08-05, under 510(k) number K181217.

Who is the listed applicant for VesoFlow Lite DVT Compression Device?

The FDA 510(k) record lists Caremed Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VesoFlow Lite DVT Compression Device?

The FDA product code for VesoFlow Lite DVT Compression Device is JOW.

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