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FDA 510(k)

MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR

K-Number: K924545 · 1992-12-01

ApplicantMod Mode Medical
Decision Date1992-12-01
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mod Mode Medical. It received FDA 510(k) clearance on 1992-12-01 under 510(k) number K924545. 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 MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR?

MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1992-12-01. The listed applicant is Mod Mode Medical. The 510(k) number is K924545.

When did MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR receive FDA 510(k) clearance?

MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR received FDA 510(k) clearance on 1992-12-01, under 510(k) number K924545.

Who is the listed applicant for MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR?

The FDA 510(k) record lists Mod Mode Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR?

The FDA product code for MICRO MODE-TRANS ELECTRICAL NEURAL STIMULATOR is GZJ.

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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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