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FDA 510(k)

VesoFlow Lite DVT Compression Device

K-Number: K181217 · 2018-08-05

ApplicantCaremed Supply, Inc.
Decision Date2018-08-05
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VesoFlow Lite DVT Compression Device is a medical device manufactured by Caremed Supply, Inc.. It received FDA 510(k) clearance on 2018-08-05 under approval number K181217. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Caremed Supply, Inc.. The 510(k) number is K181217.

When was VesoFlow Lite DVT Compression Device approved by the FDA?

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

What company makes VesoFlow Lite DVT Compression Device?

VesoFlow Lite DVT Compression Device is manufactured by Caremed Supply, Inc..

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

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

Related Clinical Trials

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Related Devices (Code: JOW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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