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MEDTRONIC AFT

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
21353943003368396MEDTRONIC AFT1N2020-04-258200 Coral Sea Street Moundsview MN US 55112

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
58241767000610K070311CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261GEI2007-04-24
58241514629171K060400CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLATGEI2006-02-28
58241465253070K043291CARDIOBLATE DISPERSIVE ELECTRODE ADAPTER (ACCESSORY), MODEL 60884GEI2004-12-21
58241089548231K013392CARDIOBLATE SURGICAL ABLATION PEN, MODEL 60811C; CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 60880OCL2002-01-25

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI32007-04-24
OCL12002-01-25