DYNATRON 800— 510(k) K932937

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K932937 for DYNATRON 800, Substantially Equivalent on 1993-10-08. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code IMG
Device class: Class 2
Regulation: 21 CFR 890.5860
Advisory panel: Physical Medicine
Date received: 1993-06-16
Decision date: 1993-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IMG

K244041 — Ultrasound Therapy Workstation (XMS-UET2)2025-10-07
K153559 — OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System2016-08-26
K150353 — BTL-40002015-11-13
K150436 — ComboRehab2015-11-13
K120217 — SONICSTIMU COMBO THERAPEUTIC DEVICE2012-11-21

More clearances from Dynatronics Corp.

K132057 — DYNATRON PELTIER THERMOSTIM PROBE2014-01-24
K113250 — DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE2012-02-09
K060814 — DYNATRON ION IONTOPHORESIS ELECTRODE2006-06-14
K051680 — DYNATRON DX2 TRACTION UNIT2005-10-11
K051261 — DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE2005-07-25

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