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FDA 510(k)

TAYLOR GENERAL PURPOSE MONITORING ELECTRODE

K-Number: K954951 · 1996-05-30

ApplicantTaylor Industries, Inc.
Decision Date1996-05-30
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TAYLOR GENERAL PURPOSE MONITORING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Taylor Industries, Inc.. It received FDA 510(k) clearance on 1996-05-30 under 510(k) number K954951. 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 TAYLOR GENERAL PURPOSE MONITORING ELECTRODE?

TAYLOR GENERAL PURPOSE MONITORING ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Taylor Industries, Inc.. The 510(k) number is K954951.

When did TAYLOR GENERAL PURPOSE MONITORING ELECTRODE receive FDA 510(k) clearance?

TAYLOR GENERAL PURPOSE MONITORING ELECTRODE received FDA 510(k) clearance on 1996-05-30, under 510(k) number K954951.

Who is the listed applicant for TAYLOR GENERAL PURPOSE MONITORING ELECTRODE?

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

What is the FDA product code for TAYLOR GENERAL PURPOSE MONITORING ELECTRODE?

The FDA product code for TAYLOR GENERAL PURPOSE MONITORING ELECTRODE 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 Taylor Industries, 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.

K941977TAYLOR LONG TERM MONITORING ELECTRODE

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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