DYNATRON 900— 510(k) K993919

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K993919 for DYNATRON 900, Substantially Equivalent on 2000-01-03. Applicant: Dynatronics Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code ITH
Device class: Class 2
Regulation: 21 CFR 890.5900
Advisory panel: Physical Medicine
Date received: 1999-11-18
Decision date: 2000-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ITH

K243775 — True Non-Surgical Spinal Decompression System (DRX9000-SL)2025-07-18
K243366 — DRX9000C-SL Cervical Spinal Decompression System2025-06-18
K214037 — Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-Trac2024-02-22
K222912 — c1Trac2023-05-16
K151640 — ELTRAC 4712015-10-16

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.