Medtronic Aft

FDA Filings

This page includes the latest FDA filings for Medtronic Aft. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number2135394
FEI Number3003368396
NameMEDTRONIC AFT
Owner & OperatorMEDTRONIC INC.
Contact Address710 Medtronic Pkwy.
Minneapolis MN 55432 US
Official Correspondent
  • CHRISTINE - BOES
  • x-763-5260396-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address8200 Coral Sea Street
Moundsview, MN 55112 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
MEDTRONIC AFT [MEDTRONIC INC.]
Cardioblate Gemini2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Cardioblate Generator2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Cardioblate Diagnostic Kit2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Dispersive Electrode Adapter2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Remote Control Foot Switch2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Dispersive Electrode Cable2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Cardioblate Surgical Ablation Pen2008-03-14
MEDTRONIC AFT [MEDTRONIC INC.]
Cardioblate Surgical Abl Generator2008-03-14

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