FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DYNATRON ION IONTOPHORESIS ELECTRODE

K Number: K060814 · Decision Jun 14, 2006
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
72
Applicant Total
24
Review Days
79

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Basic Information

Device Name
DYNATRON ION IONTOPHORESIS ELECTRODE
K Number
K060814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5525
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dynatronics Corp.
Date Received
March 27, 2006
Decision Date
June 14, 2006
Product Code
EGJ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EGJ Device, Iontophoresis, Other Uses

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Other Clearances by Dynatronics Corp.

K Number Device Name
K132057 DYNATRON PELTIER THERMOSTIM PROBE
K113250 DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE
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)
K010948 DYNATRON STS RX
K010565 DYNATRON STS
K993919 DYNATRON 900
Search all 24 clearances from Dynatronics Corp. →