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FDA 510(k)

myPatch-s

K-Number: K160704 · 2016-07-15

ApplicantDms-Service, LLC
Decision Date2016-07-15
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

myPatch-s is a medical device manufactured by Dms-Service, LLC. It received FDA 510(k) clearance on 2016-07-15 under approval number K160704. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the myPatch-s?

myPatch-s is a medical device that received FDA 510(k) clearance on 2016-07-15. It is manufactured by Dms-Service, LLC. The 510(k) number is K160704.

When was myPatch-s approved by the FDA?

myPatch-s received FDA 510(k) clearance on 2016-07-15, under approval number K160704.

What company makes myPatch-s?

myPatch-s is manufactured by Dms-Service, LLC.

What is the FDA product code for myPatch-s?

The FDA product code for myPatch-s is DSH.

Other Devices by Dms-Service, LLC

K163535my Patch sl

Related Devices (Code: DSH)

K162571Bioflux SoftwareBiotricity, Inc. K171936Peerbridge Cor(TM) SystemPeerbridge Health, Inc. K162503Stealth System, Stealth Sensor, Stealth Smart Cable, StealthView SoftwareCardiac Insight, Inc. K163535my Patch slDms-Service, LLC K173461ECG recorder and Arrhythmia DetectorSmart Solutions Technologies SL K172862Portable ECG Monitor (ECG3)Andon Health Co, Ltd.

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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