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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