DYNATRON 400— 510(k) K924319

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K924319 for DYNATRON 400, Substantially Equivalent on 1993-01-14. 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: 1992-08-13
Decision date: 1993-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIH

K231575 — Vecttor VT-3002024-02-08
K202725 — ETD40002021-03-26
K183692 — Avid IF22019-06-12
K122944 — GEMORE TRUE SINE INTERFERENTIAL STIMULATOR2012-12-21
K121662 — VECTTOR VT-2002012-11-21

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.