FDA.reportPublic FDA data

Carrie Schleis

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30089739403008973940Carrie Schleis1N2027-01-018200 Coral Sea St NE Mounds View MN US 55112

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1269131232151429P980035MEDTRONIC KAPPA 700/600 SERIES PULSE GENERATORS AND MODEL 9953 SOFTWARENVZ1999-01-29
1269131620496774P930039MEDTRONIC(R) CAPSUREFIX LEAD MODEL 4068,4067,4568NVN1996-03-29
1269131832008425P830061STEROID TIP(TM) MODEL 4503&4003 TRANSVENOUS PACINGNVN1986-07-29
1269131410889433P090013REVO MRI SURESCAN IPG AND PACING SYSTEMLWP2011-02-08
1269132066997381K240693LINQ II™ Insertable Cardiac Monitor (ICM)MXD2024-03-28
1269131221331976K233320LINQ II™ Insertable Cardiac Monitor (LNQ22)MXD2023-10-31
1269131640107660K221962LINQ II Insertable Cardiac MonitorMXD2022-08-25
1269131305795452K212008Reveal LINQ Insertable Cardiac MonitorMXD2021-07-22
1269131821575444K211304LINQ II Insertable Cardiac MonitorMXD2021-05-28
1269131140411658K200795LINQ II Insertable Cardiac Monitor, LINQ Mobile Manager, Device Command Library, Instrument Command Library, LINQ Tool KitMXD2020-07-03
1269131481378810K162855Reveal LINQMXD2017-02-23

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MXD72024-03-28
NVN21996-03-29
LWP12011-02-08
NVZ11999-01-29