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FDA 510(k)

Devon 52 Sequential Compression Device

K-Number: K182150 · 2018-12-18

Decision Date2018-12-18
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Devon 52 Sequential Compression Device is a medical device manufactured by Devon Medical Products (Jiangsu), Ltd.. It received FDA 510(k) clearance on 2018-12-18 under approval number K182150. 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 Devon 52 Sequential Compression Device?

Devon 52 Sequential Compression Device is a medical device that received FDA 510(k) clearance on 2018-12-18. It is manufactured by Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K182150.

When was Devon 52 Sequential Compression Device approved by the FDA?

Devon 52 Sequential Compression Device received FDA 510(k) clearance on 2018-12-18, under approval number K182150.

What company makes Devon 52 Sequential Compression Device?

Devon 52 Sequential Compression Device is manufactured by Devon Medical Products (Jiangsu), Ltd..

What is the FDA product code for Devon 52 Sequential Compression Device?

The FDA product code for Devon 52 Sequential Compression Device is JOW.

Related Clinical Trials

Other Devices by Devon Medical Products (Jiangsu), Ltd.

Related Devices (Code: JOW)

Official Source

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