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 500

K-Number: K870947 · 1987-08-18

ApplicantDynatronics Corp.
Decision Date1987-08-18
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRON 500 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1987-08-18 under 510(k) number K870947. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON 500?

DYNATRON 500 is a medical device that received FDA 510(k) clearance on 1987-08-18. The listed applicant is Dynatronics Corp.. The 510(k) number is K870947.

When did DYNATRON 500 receive FDA 510(k) clearance?

DYNATRON 500 received FDA 510(k) clearance on 1987-08-18, under 510(k) number K870947.

Who is the listed applicant for DYNATRON 500?

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 500?

The FDA product code for DYNATRON 500 is IPF.

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: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

↑