FDA 510(k)

Chattanooga Revolution Wireless

K-Number: K153696 · 2016-04-14

Decision Date2016-04-14

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Chattanooga Revolution Wireless is a medical device manufactured by Djo, LLC. It received FDA 510(k) clearance on 2016-04-14 under approval number K153696. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Chattanooga Revolution Wireless?

Chattanooga Revolution Wireless is a medical device that received FDA 510(k) clearance on 2016-04-14. It is manufactured by Djo, LLC. The 510(k) number is K153696.

When was Chattanooga Revolution Wireless approved by the FDA?

Chattanooga Revolution Wireless received FDA 510(k) clearance on 2016-04-14, under approval number K153696.

What company makes Chattanooga Revolution Wireless?

Chattanooga Revolution Wireless is manufactured by Djo, LLC.

What is the FDA product code for Chattanooga Revolution Wireless?

The FDA product code for Chattanooga Revolution Wireless is IPF.

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Related Devices (Code: IPF)

K160614Xcite Clinical StationRestorative Therapies, Inc. K163067CyMedica e-vive System; CY-1000Cymedica Orthopedics, Inc. K160992HPM-6000BTL Industries, Inc. K151922StimSox(TM) SystemStimmed, LLC K160299geko(TM) Plus R-2 Neuromuscular StimulatorFirstkind Limited K153224VitalStim(R) Plus Electrotherapy SystemDjo, LLC

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.