FDA 510(k)

EVERYWAY LOW BACK PAIN RELIEF SYSTEM

K-Number: K110716 · 2011-10-18

ApplicantEveryway Medical Instruments Co.,Ltd

Decision Date2011-10-18

Product CodeNUH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EVERYWAY LOW BACK PAIN RELIEF SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Everyway Medical Instruments Co.,Ltd. It received FDA 510(k) clearance on 2011-10-18 under 510(k) number K110716. 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 EVERYWAY LOW BACK PAIN RELIEF SYSTEM?

EVERYWAY LOW BACK PAIN RELIEF SYSTEM is a medical device that received FDA 510(k) clearance on 2011-10-18. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K110716.

When did EVERYWAY LOW BACK PAIN RELIEF SYSTEM receive FDA 510(k) clearance?

EVERYWAY LOW BACK PAIN RELIEF SYSTEM received FDA 510(k) clearance on 2011-10-18, under 510(k) number K110716.

Who is the listed applicant for EVERYWAY LOW BACK PAIN RELIEF SYSTEM?

The FDA 510(k) record lists Everyway Medical Instruments Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVERYWAY LOW BACK PAIN RELIEF SYSTEM?

The FDA product code for EVERYWAY LOW BACK PAIN RELIEF SYSTEM is NUH.

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Related Devices (Code: NUH)

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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.