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FDA 510(k)

WALLANT NEUROLOGIX GENERAL PURPOSE TENS

K-Number: K860847 · 1986-08-07

ApplicantWallant Intl. Trade, Inc.
Decision Date1986-08-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

WALLANT NEUROLOGIX GENERAL PURPOSE TENS is the device name listed in this FDA 510(k) record. The listed applicant is Wallant Intl. Trade, Inc.. It received FDA 510(k) clearance on 1986-08-07 under 510(k) number K860847. 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 WALLANT NEUROLOGIX GENERAL PURPOSE TENS?

WALLANT NEUROLOGIX GENERAL PURPOSE TENS is a medical device that received FDA 510(k) clearance on 1986-08-07. The listed applicant is Wallant Intl. Trade, Inc.. The 510(k) number is K860847.

When did WALLANT NEUROLOGIX GENERAL PURPOSE TENS receive FDA 510(k) clearance?

WALLANT NEUROLOGIX GENERAL PURPOSE TENS received FDA 510(k) clearance on 1986-08-07, under 510(k) number K860847.

Who is the listed applicant for WALLANT NEUROLOGIX GENERAL PURPOSE TENS?

The FDA 510(k) record lists Wallant Intl. Trade, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALLANT NEUROLOGIX GENERAL PURPOSE TENS?

The FDA product code for WALLANT NEUROLOGIX GENERAL PURPOSE TENS is GZJ.

Related Clinical Trials

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Other records listing Wallant Intl. Trade, Inc. 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.

K861119WALLANT NEUROLOGIX DUAL PUR NERVE/NEUROMUSCU STIMUK810262AUTOMATIC ELECTRODE PLACEMENT BELT

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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