DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)— 510(k) K031329

Name: FDA 510(k) clearance K031329
Creator: U.S. Food and Drug Administration
Published: 2003-10-22

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K031329 for DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY), Substantially Equivalent on 2003-10-22. 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: 2003-04-28
Decision date: 2003-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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