DYNATRON 525— 510(k) K961261

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K961261 for DYNATRON 525, Substantially Equivalent on 1996-09-05. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1996-04-02
Decision date: 1996-09-05
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.