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FDA 510(k)

RF1400 Active Compression Wrap

K-Number: K162481 · 2017-02-16

ApplicantRecovery Force, LLC
Decision Date2017-02-16
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RF1400 Active Compression Wrap is the device name listed in this FDA 510(k) record. The listed applicant is Recovery Force, LLC. It received FDA 510(k) clearance on 2017-02-16 under 510(k) 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. The listed applicant is Recovery Force, LLC. The 510(k) number is K162481.

When did RF1400 Active Compression Wrap receive FDA 510(k) clearance?

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

Who is the listed applicant for RF1400 Active Compression Wrap?

The FDA 510(k) record lists Recovery Force, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Recovery Force, LLC 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.

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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.

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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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