DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE— 510(k) K113250

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K113250 for DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE, Substantially Equivalent on 2012-02-09. Applicant: Dynatronics Corp..

Clearance details

Applicant: Dynatronics Corp.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2011-11-03
Decision date: 2012-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.