DYNATRON 125 ULTRASOUND— 510(k) K961250

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K961250 for DYNATRON 125 ULTRASOUND, Substantially Equivalent on 1996-08-26. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 1996-04-01
Decision date: 1996-08-26
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.