DYNATRON ION IONTOPHORESIS ELECTRODE— 510(k) K060814

Name: FDA 510(k) clearance K060814
Creator: U.S. Food and Drug Administration
Published: 2006-06-14

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K060814 for DYNATRON ION IONTOPHORESIS ELECTRODE, Substantially Equivalent on 2006-06-14. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2006-03-27
Decision date: 2006-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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