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. The listed applicant is Devon Medical Products (Jiangsu), Ltd.. The 510(k) number is K182150.
When did Devon 52 Sequential Compression Device receive FDA 510(k) clearance?
Devon 52 Sequential Compression Device received FDA 510(k) clearance on 2018-12-18, under 510(k) number K182150.
Who is the listed applicant for Devon 52 Sequential Compression Device?
The FDA 510(k) record lists Devon Medical Products (Jiangsu), Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Devon 52 Sequential Compression Device?
The FDA product code for Devon 52 Sequential Compression Device is JOW.
Other records listing Devon Medical Products (Jiangsu), Ltd. as applicant
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.
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.
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.