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FDA 510(k)

VenAir, Sequential Compression System

K-Number: K213577 · 2022-06-28

ApplicantApex Medical Corp.
Decision Date2022-06-28
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VenAir, Sequential Compression System is a medical device manufactured by Apex Medical Corp.. It received FDA 510(k) clearance on 2022-06-28 under approval number K213577. 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 VenAir, Sequential Compression System?

VenAir, Sequential Compression System is a medical device that received FDA 510(k) clearance on 2022-06-28. It is manufactured by Apex Medical Corp.. The 510(k) number is K213577.

When was VenAir, Sequential Compression System approved by the FDA?

VenAir, Sequential Compression System received FDA 510(k) clearance on 2022-06-28, under approval number K213577.

What company makes VenAir, Sequential Compression System?

VenAir, Sequential Compression System is manufactured by Apex Medical Corp..

What is the FDA product code for VenAir, Sequential Compression System?

The FDA product code for VenAir, Sequential Compression System is 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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