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FDA 510(k)

NERVE STIMULATOR, ELEC. TRANSCUTANEOUS

K-Number: K772224 · 1977-12-15

ApplicantStimulation Technology, Inc.
Decision Date1977-12-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NERVE STIMULATOR, ELEC. TRANSCUTANEOUS 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 1977-12-15 under 510(k) number K772224. 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 NERVE STIMULATOR, ELEC. TRANSCUTANEOUS?

NERVE STIMULATOR, ELEC. TRANSCUTANEOUS is a medical device that received FDA 510(k) clearance on 1977-12-15. The listed applicant is Stimulation Technology, Inc.. The 510(k) number is K772224.

When did NERVE STIMULATOR, ELEC. TRANSCUTANEOUS receive FDA 510(k) clearance?

NERVE STIMULATOR, ELEC. TRANSCUTANEOUS received FDA 510(k) clearance on 1977-12-15, under 510(k) number K772224.

Who is the listed applicant for NERVE STIMULATOR, ELEC. TRANSCUTANEOUS?

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 NERVE STIMULATOR, ELEC. TRANSCUTANEOUS?

The FDA product code for NERVE STIMULATOR, ELEC. TRANSCUTANEOUS is GZJ.

Related Clinical Trials

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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 ELECTRODEK781565ELECTRICAL NERVE STIMULATOR MODEL 6035K770447EPC 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

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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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