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FDA 510(k)

STIMULATORS, NERVE, ELECTRICAL

K-Number: K780698 · 1978-05-12

ApplicantMed General
Decision Date1978-05-12
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMULATORS, NERVE, ELECTRICAL is the device name listed in this FDA 510(k) record. The listed applicant is Med General. It received FDA 510(k) clearance on 1978-05-12 under 510(k) number K780698. 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 STIMULATORS, NERVE, ELECTRICAL?

STIMULATORS, NERVE, ELECTRICAL is a medical device that received FDA 510(k) clearance on 1978-05-12. The listed applicant is Med General. The 510(k) number is K780698.

When did STIMULATORS, NERVE, ELECTRICAL receive FDA 510(k) clearance?

STIMULATORS, NERVE, ELECTRICAL received FDA 510(k) clearance on 1978-05-12, under 510(k) number K780698.

Who is the listed applicant for STIMULATORS, NERVE, ELECTRICAL?

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

What is the FDA product code for STIMULATORS, NERVE, ELECTRICAL?

The FDA product code for STIMULATORS, NERVE, ELECTRICAL is GZJ.

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Other records listing Med General 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.

K791097CEPTORTRODE WITH CEPTOR HESIVEK791098SINGLE-USE MINI-BULLDOGK790763MAXI-VAC TMK790269CEPTOR HESIVEK782006MEDGENERAL SINGLE-USE BULLDOGK781239MYO-STIM

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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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