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FDA 510(k)

ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607

K-Number: K033544 · 2003-12-10

ApplicantEveryway Medical Instruments Co.,Ltd
Decision Date2003-12-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607 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 2003-12-10 under 510(k) number K033544. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607?

ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607 is a medical device that received FDA 510(k) clearance on 2003-12-10. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K033544.

When did ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607 receive FDA 510(k) clearance?

ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607 received FDA 510(k) clearance on 2003-12-10, under 510(k) number K033544.

Who is the listed applicant for ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607?

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 ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607?

The FDA product code for ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607 is IPF.

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Related Devices (Code: IPF)

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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.

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