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FDA 510(k)

EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR

K-Number: K071624 · 2007-11-27

ApplicantEverlife Medical Equipment Co., Ltd.
Decision Date2007-11-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Everlife Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2007-11-27 under 510(k) number K071624. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR?

EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 2007-11-27. The listed applicant is Everlife Medical Equipment Co., Ltd.. The 510(k) number is K071624.

When did EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR receive FDA 510(k) clearance?

EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR received FDA 510(k) clearance on 2007-11-27, under 510(k) number K071624.

Who is the listed applicant for EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR?

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

What is the FDA product code for EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR?

The FDA product code for EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR is GZJ.

Related Clinical Trials

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.

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Other records listing Everlife Medical Equipment Co., Ltd. as applicant

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.

K071320EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311K070890EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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