FDA.reportPublic FDA data

John Skousen

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
10001659711000165971John Skousen1N2026-01-015677 AIRLINE ROAD REGULATORY AFFAIRS, C/O DWYNDL NELMS Arlington TN US 38002
30081596163008159616John Skousen1N2026-01-015677 Airline Road Regulatory Affairs, c/o John Skuosen (MicroPort Arlington TN US 38002

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1246691092071576P980049DEFENDER II MODEL 9201 IMPLANTABLE CARDIOVERTER DEFIBRILLATORMRM1999-09-15
223971408552604P980049DEFENDER II MODEL 9201 IMPLANTABLE CARDIOVERTER DEFIBRILLATORMRM1999-09-15
1246691192174973P950029CHORUS RM MODEL 7034 DDDR PACEMAKER INCL. OPUS RM MODEL 4534 SSIR PACEMAKERDXY1997-03-10
223971783478394P950029CHORUS RM MODEL 7034 DDDR PACEMAKER INCL. OPUS RM MODEL 4534 SSIR PACEMAKERDXY1997-03-10
223971508059278P130010VEGA Steroid-Eluting Endocardial Leads (VEGA™ R45, VEGA™ R52, and VEGA™ R58)NVN2023-05-17
1246691833779844P130010VEGA Steroid-Eluting Endocardial Leads (VEGA™ R45, VEGA™ R52, and VEGA™ R58)NVN2023-05-17
223971352179517P060027OVATIO CRT SYSTEMNIK2008-05-15
1246691876825892P060027OVATIO CRT SYSTEMNIK2008-05-15
223971488886398K042002SYNESCOPE, EASYSCOPE, SYNECOM, HOLTERREADERDQK2004-10-20
1246691554919794K042002SYNESCOPE, EASYSCOPE, SYNECOM, HOLTERREADERDQK2004-10-20
1246691815368851K032466SPIDERVIEWMWJ2003-08-22
223972026658110K032466SPIDERVIEWMWJ2003-08-22
1246691088661542
223971105877156
223971941225855

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DQK32004-10-20
MWJ32003-08-22
NIK22008-05-15
MRM21999-09-15
DXY21997-03-10