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FDA 510(k)

MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR

K-Number: K884032 · 1988-10-13

ApplicantMorgan Associates, Inc.
Decision Date1988-10-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Morgan Associates, Inc.. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K884032. 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 MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Morgan Associates, Inc.. The 510(k) number is K884032.

When did MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR receive FDA 510(k) clearance?

MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR received FDA 510(k) clearance on 1988-10-13, under 510(k) number K884032.

Who is the listed applicant for MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

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

What is the FDA product code for MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR?

The FDA product code for MORGAN TRANSCUTANEOUS ELECTRICAL NERVE 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 Morgan Associates, 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.

K832005JP-2 RESPIRATORY MONITORING SYSTEM

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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