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FDA 510(k)

DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)

K-Number: K864370 · 1987-04-10

ApplicantDynatronics Laser Corp.
Decision Date1987-04-10
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent for Some Indications

Device Summary

DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR) is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Laser Corp.. It received FDA 510(k) clearance on 1987-04-10 under 510(k) number K864370. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)?

DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR) is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Dynatronics Laser Corp.. The 510(k) number is K864370.

When did DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR) receive FDA 510(k) clearance?

DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR) received FDA 510(k) clearance on 1987-04-10, under 510(k) number K864370.

Who is the listed applicant for DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)?

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

What is the FDA product code for DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)?

The FDA product code for DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR) 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 Dynatronics Laser Corp. 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.

K920939DYNATRON 300 ULRASOUNDK900639DYNATRON 350 EMG/BIOFEEDBACK ANALYZERK900321DYNATRON 330 BODY COMPOSITION ANALYZERK880464DYNATRON II

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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