Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DYNATRON 650

K-Number: K950348 · 1995-09-13

ApplicantDynatronics Corp.
Decision Date1995-09-13
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent for Some Indications

Device Summary

DYNATRON 650 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1995-09-13 under 510(k) number K950348. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DYNATRON 650?

DYNATRON 650 is a medical device that received FDA 510(k) clearance on 1995-09-13. The listed applicant is Dynatronics Corp.. The 510(k) number is K950348.

When did DYNATRON 650 receive FDA 510(k) clearance?

DYNATRON 650 received FDA 510(k) clearance on 1995-09-13, under 510(k) number K950348.

Who is the listed applicant for DYNATRON 650?

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 650?

The FDA product code for DYNATRON 650 is LIH.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 23 devices →

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.

↑