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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 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.

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. 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.

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.K250974Bio Arterial Deluxe (IC-BAP-DX)Bio Compression Systems, Inc.K250190Sequential Compression System (SCD600)Shenzhen Comen Medical Instruments Co.,Ltd

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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