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FDA 510(k)

TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR

K-Number: K884972 · 1989-07-27

ApplicantFuturemed Div. of Future Impex Corp.
Decision Date1989-07-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1989-07-27 under 510(k) number K884972. 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 TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR?

TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR is a medical device that received FDA 510(k) clearance on 1989-07-27. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K884972.

When did TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR receive FDA 510(k) clearance?

TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR received FDA 510(k) clearance on 1989-07-27, under 510(k) number K884972.

Who is the listed applicant for TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR?

The FDA 510(k) record lists Futuremed Div. of Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR?

The FDA product code for TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR is GZJ.

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Other records listing Futuremed Div. of Future Impex Corp. as applicant

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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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