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FDA 510(k)

DYNATRON 525

K-Number: K961261 · 1996-09-05

ApplicantDynatronics Corp.
Decision Date1996-09-05
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DYNATRON 525 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1996-09-05 under 510(k) number K961261. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON 525?

DYNATRON 525 is a medical device that received FDA 510(k) clearance on 1996-09-05. The listed applicant is Dynatronics Corp.. The 510(k) number is K961261.

When did DYNATRON 525 receive FDA 510(k) clearance?

DYNATRON 525 received FDA 510(k) clearance on 1996-09-05, under 510(k) number K961261.

Who is the listed applicant for DYNATRON 525?

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

What is the FDA product code for DYNATRON 525?

The FDA product code for DYNATRON 525 is LIH.

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Other records listing Dynatronics 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.

K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK060814DYNATRON ION IONTOPHORESIS ELECTRODEK051680DYNATRON DX2 TRACTION UNITK051261DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEK043047DYNATRON IBOX IONTOPHORESIS DEVICEK040729SOLARIS D890 THERAPY PROBE

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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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