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FDA 510(k)

StimPlus Patch, StimPlus Patch, StimPlus Patch

K-Number: K200561 · 2020-07-01

ApplicantJkh Health Co., Ltd.
Decision Date2020-07-01
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

StimPlus Patch, StimPlus Patch, StimPlus Patch is a medical device manufactured by Jkh Health Co., Ltd.. It received FDA 510(k) clearance on 2020-07-01 under approval number K200561. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the StimPlus Patch, StimPlus Patch, StimPlus Patch?

StimPlus Patch, StimPlus Patch, StimPlus Patch is a medical device that received FDA 510(k) clearance on 2020-07-01. It is manufactured by Jkh Health Co., Ltd.. The 510(k) number is K200561.

When was StimPlus Patch, StimPlus Patch, StimPlus Patch approved by the FDA?

StimPlus Patch, StimPlus Patch, StimPlus Patch received FDA 510(k) clearance on 2020-07-01, under approval number K200561.

What company makes StimPlus Patch, StimPlus Patch, StimPlus Patch?

StimPlus Patch, StimPlus Patch, StimPlus Patch is manufactured by Jkh Health Co., Ltd..

What is the FDA product code for StimPlus Patch, StimPlus Patch, StimPlus Patch?

The FDA product code for StimPlus Patch, StimPlus Patch, StimPlus Patch is NUH.

Other Devices by Jkh Health Co., Ltd.

K153520Electronic Pulse Stimulator K162517Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13 K202839Overlapped Compression Therapy K211050Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304 K223541Cold/Hot Compression K240986Cold Compression

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Related Devices (Code: NUH)

K162630CP Relief Wand-OTCMid-America Medical Innovations, LLC K161453WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605AWell-Life Healthcare Limited K160508Electronic Pulse StimulatorBeijing Choice Electronic Technololgy Co., Ltd. K161537OTC TENS Device, Model PTS-IVCounter Scientific Development (Gz), Ltd. K151995Painmaster MCT PatchNewmark, Inc. K160255HBOTC Muscle and Nerve StimulatorHb Medical, Inc.

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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