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FDA 510(k)

RF1400 Active Compression Wrap

K-Number: K162481 · 2017-02-16

Decision Date2017-02-16
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RF1400 Active Compression Wrap is a medical device manufactured by Recovery Force, LLC. It received FDA 510(k) clearance on 2017-02-16 under approval number K162481. 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 RF1400 Active Compression Wrap?

RF1400 Active Compression Wrap is a medical device that received FDA 510(k) clearance on 2017-02-16. It is manufactured by Recovery Force, LLC. The 510(k) number is K162481.

When was RF1400 Active Compression Wrap approved by the FDA?

RF1400 Active Compression Wrap received FDA 510(k) clearance on 2017-02-16, under approval number K162481.

What company makes RF1400 Active Compression Wrap?

RF1400 Active Compression Wrap is manufactured by Recovery Force, LLC.

What is the FDA product code for RF1400 Active Compression Wrap?

The FDA product code for RF1400 Active Compression Wrap is JOW.

Related Clinical Trials

Other Devices by Recovery Force, LLC

Related Devices (Code: JOW)

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.