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FDA 510(k)

Devon 51

K-Number: K172030 · 2017-11-27

ApplicantDevon Medical Products (Jiangsu), Ltd.
Decision Date2017-11-27
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Devon 51 is a medical device manufactured by Devon Medical Products (Jiangsu), Ltd.. It received FDA 510(k) clearance on 2017-11-27 under approval number K172030. 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 51?

Devon 51 is a medical device that received FDA 510(k) clearance on 2017-11-27. It is manufactured by Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K172030.

When was Devon 51 approved by the FDA?

Devon 51 received FDA 510(k) clearance on 2017-11-27, under approval number K172030.

What company makes Devon 51?

Devon 51 is manufactured by Devon Medical Products (Jiangsu), Ltd..

What is the FDA product code for Devon 51?

The FDA product code for Devon 51 is JOW.

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

K170814Devon 24 K182150Devon 52 Sequential Compression Device K173528Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System K190423Devon 24D Deep Vein Thrombosis (DVT) Prevention Therapy System K182578Devon 62 Deep Vein Thrombosis (DVT) Prevention Therapy Device

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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