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FDA 510(k) Application Details - K060814
Device Classification Name
Device, Iontophoresis, Other Uses
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510(K) Number
K060814
Device Name
Device, Iontophoresis, Other Uses
Applicant
DYNATRONICS CORP.
7030 PARK CENTRE DR.
SALT LAKE CITY, UT 84121 US
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Contact
KELVYN CULLIMORE, JR
Other 510(k) Applications for this Contact
Regulation Number
890.5525
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Classification Product Code
EGJ
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More FDA Info for this Product Code
Date Received
03/27/2006
Decision Date
06/14/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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