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FDA 510(k) Applications Submitted by John Ives
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060189
01/24/2006
PEDIATRIC SUBDERMAL WIRE ELECTRODE (PSWE)
IVES EEG SOLUTIONS, INC.
K171102
04/13/2017
Ives MR Conditional Cup Electrode
Ives EGG Solutions
K071118
04/20/2007
GOLD CUP ELECTRODE, SILVER CUP ELECTRODE AND ELECTRODE WITH AG-AG/CL COATING AND CONDUCTIVE PLASTIC ELECTRODE
IVES EEG SOLUTIONS, INC.
K062880
09/26/2006
SUBDERMAL WIRE ELECTRODE, MODEL SWE
IVES EEG SOLUTIONS, INC.
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