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FDA 510(k)

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908

K-Number: K110509 · 2011-06-20

ApplicantEveryway Medical Instruments Co.,Ltd
Decision Date2011-06-20
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 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 2011-06-20 under 510(k) number K110509. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908?

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 is a medical device that received FDA 510(k) clearance on 2011-06-20. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K110509.

When did EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 receive FDA 510(k) clearance?

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 received FDA 510(k) clearance on 2011-06-20, under 510(k) number K110509.

Who is the listed applicant for EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908?

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 INTERFERNTIAL STIMULATOR, MODEL IF-908?

The FDA product code for EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908 is LIH.

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Other records listing Everyway Medical Instruments Co.,Ltd as applicant

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Related Devices (Code: LIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK100246MAX-IF1000Bio Protech, 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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