DYNATRON 300 ULRASOUND— 510(k) K920939

Substantially Equivalent

Dynatronics Laser Corp.

FDA 510(k) clearance K920939 for DYNATRON 300 ULRASOUND, Substantially Equivalent on 1993-03-04. Applicant: Dynatronics Laser Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Laser Corp.
Product code: Code IMG
Device class: Class 2
Regulation: 21 CFR 890.5860
Advisory panel: Physical Medicine
Date received: 1992-02-27
Decision date: 1993-03-04
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.