Dynatronics Corp.
Dynatronics Corp. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2014.
Top product codes for Dynatronics Corp.
Recent clearances by Dynatronics Corp.
- K132057 — DYNATRON PELTIER THERMOSTIM PROBE
- K113250 — DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE
- K060814 — DYNATRON ION IONTOPHORESIS ELECTRODE
- K051680 — DYNATRON DX2 TRACTION UNIT
- K051261 — DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE
- K043047 — DYNATRON IBOX IONTOPHORESIS DEVICE
- K040729 — SOLARIS D890 THERAPY PROBE
- K031329 — DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)
- K010565 — DYNATRON STS
- K010948 — DYNATRON STS RX
- K993919 — DYNATRON 900
- K961261 — DYNATRON 525
- K961250 — DYNATRON 125 ULTRASOUND
- K950348 — DYNATRON 650
- K950349 — DYNATRON 950
- K941577 — DYNATRON 550
- K944935 — DYNATRON 250
- K935728 — DYNATRON 150
- K932937 — DYNATRON 800
- K924319 — DYNATRON 400
- K903577 — DYNATRON 200 MICROCURRENT
- K897178 — DYNATRON 360 RANGE OF MOTION TESTING DEVICE
- K880912 — DYNATRON 2000
- K870947 — DYNATRON 500
Data sourced from openFDA. This site is unofficial and independent of the FDA.