Devon 52 Sequential Compression Device
K-Number: K182150 · 2018-12-18
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.