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FDA 510(k)

ELECTREAT MODEL 250 TRANSCUTANEOUS STIM

K-Number: K790189 · 1979-02-08

ApplicantElectreat, Inc.
Decision Date1979-02-08
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTREAT MODEL 250 TRANSCUTANEOUS STIM is the device name listed in this FDA 510(k) record. The listed applicant is Electreat, Inc.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790189. 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 ELECTREAT MODEL 250 TRANSCUTANEOUS STIM?

ELECTREAT MODEL 250 TRANSCUTANEOUS STIM is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Electreat, Inc.. The 510(k) number is K790189.

When did ELECTREAT MODEL 250 TRANSCUTANEOUS STIM receive FDA 510(k) clearance?

ELECTREAT MODEL 250 TRANSCUTANEOUS STIM received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790189.

Who is the listed applicant for ELECTREAT MODEL 250 TRANSCUTANEOUS STIM?

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

What is the FDA product code for ELECTREAT MODEL 250 TRANSCUTANEOUS STIM?

The FDA product code for ELECTREAT MODEL 250 TRANSCUTANEOUS STIM 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 Electreat, 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.

K791158STIMULATOR, ELECTRICAL NERVE

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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