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FDA 510(k)

RecoveryRx

K-Number: K190251 · 2019-06-28

ApplicantBioelectronics Corporation
Decision Date2019-06-28
Product CodeILX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RecoveryRx is a medical device manufactured by Bioelectronics Corporation. It received FDA 510(k) clearance on 2019-06-28 under approval number K190251. The device is classified under product code ILX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RecoveryRx?

RecoveryRx is a medical device that received FDA 510(k) clearance on 2019-06-28. It is manufactured by Bioelectronics Corporation. The 510(k) number is K190251.

When was RecoveryRx approved by the FDA?

RecoveryRx received FDA 510(k) clearance on 2019-06-28, under approval number K190251.

What company makes RecoveryRx?

RecoveryRx is manufactured by Bioelectronics Corporation.

What is the FDA product code for RecoveryRx?

The FDA product code for RecoveryRx is ILX.

Other Devices by Bioelectronics Corporation

K152432ActiPatch(R) K192234ActiPatch

Related Devices (Code: ILX)

K202337Pulsed electromagnetic field wrapHi-Dow International, Inc. K241395Active System; Avenue8Caerus Corporation

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.

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