Ives Eeg Solutions, Inc. is one of 680 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Ives Eeg Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GOLD CUP ELECTRODE, SILVER CUP ELECTRODE AND ELECTRODE WITH AG-AG/CL COATING AND CONDUCTIVE PLASTIC ELECTRODE, SUBDERMAL WIRE ELECTRODE, MODEL SWE, PEDIATRIC SUBDERMAL WIRE ELECTRODE (PSWE)
3
Total
3
Cleared
0
Denied
Ives Eeg Solutions, Inc. has 3 FDA 510(k) cleared medical devices. Based in Manotick, Ontario, CA.
Historical record: 3 cleared submissions from 2006 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ives Eeg Solutions, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ives Eeg Solutions, Inc.
3 devices