Ives Eeg Solutions Inc

FDA Filings

This page includes the latest FDA filings for Ives Eeg Solutions Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008806011
FEI Number3008806011
NameIves EEG Solutions
Owner & OperatorIVES EEG SOLUTIONS, INC.
Contact Address25 Storey Ave #118
Newburyport MA 01950 US
Official Correspondent
  • JOHN R IVES
  • x-978-3588006-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address44 Merrimac St
Newburyport, MA 01950 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Ives EEG Solutions [IVES EEG SOLUTIONS, INC.]
Cutaneous EEG Electrode2007-11-06
Ives EEG Solutions [IVES EEG SOLUTIONS, INC.]
Subdermal Wire Electrode2007-11-06
IVES EEG SOLUTIONS, INC.
GOLD CUP ELECTRODE, SILVER CUP ELECTRODE AND ELECTRODE WITH AG-AG/CL COATING AND CONDUCTIVE PLASTIC ELECTRODE2007-09-07
IVES EEG SOLUTIONS, INC.
SUBDERMAL WIRE ELECTRODE, MODEL SWE2006-12-22
Ives EEG Solutions [IVES EEG SOLUTIONS, INC.]
PEDIATRIC SUBDERMAL2006-08-28
IVES EEG SOLUTIONS, INC.
PEDIATRIC SUBDERMAL WIRE ELECTRODE (PSWE)2006-05-30

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