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FDA 510(k)

ELECTRICAL NERVE STIMULATOR MODEL 6035

K-Number: K781565 · 1978-10-11

ApplicantStimulation Technology, Inc.
Decision Date1978-10-11
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRICAL NERVE STIMULATOR MODEL 6035 is the device name listed in this FDA 510(k) record. The listed applicant is Stimulation Technology, Inc.. It received FDA 510(k) clearance on 1978-10-11 under 510(k) number K781565. 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 ELECTRICAL NERVE STIMULATOR MODEL 6035?

ELECTRICAL NERVE STIMULATOR MODEL 6035 is a medical device that received FDA 510(k) clearance on 1978-10-11. The listed applicant is Stimulation Technology, Inc.. The 510(k) number is K781565.

When did ELECTRICAL NERVE STIMULATOR MODEL 6035 receive FDA 510(k) clearance?

ELECTRICAL NERVE STIMULATOR MODEL 6035 received FDA 510(k) clearance on 1978-10-11, under 510(k) number K781565.

Who is the listed applicant for ELECTRICAL NERVE STIMULATOR MODEL 6035?

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

What is the FDA product code for ELECTRICAL NERVE STIMULATOR MODEL 6035?

The FDA product code for ELECTRICAL NERVE STIMULATOR MODEL 6035 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stimulation Technology, 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.

K791048STIMTECH NEUROMUSCULAR STIMULATOR, C 600K790345STIMTECH TENS ELECTRODEK772224NERVE STIMULATOR, ELEC. TRANSCUTANEOUSK770447EPC INSTICKSK770448INS - T.E.N.S.

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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