FDA.reportPublic FDA data

Christopher Horton

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30044782763004478276Christopher Horton1N2026-01-019800 Pyramid Ct Ste 400 Englewood CO US 80112
30056876333005687633Christopher Horton1N2026-01-019800 Pyramid Ct Ste 400 Englewood CO US 80112

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
247761079368827P900060CARBOMEDICS PROSTHETIC HEART VALVE (CPHV)LWQ1993-09-29
247761011252348P150011PERCEVAL SUTURELESS HEART VALVELWR2016-01-08
692691797428474P130011FREEDOM SOLO STENTLESS HEART VALVELWR2014-06-24
247761494824805K951368CARBOMEDICS EXENDED MITRAL ROTATORMOP1995-06-20
247761502390663K260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGKRH2026-04-14
247761907158458K230318Memo 3D Semirigid Annuloplasty Ring; Memo 3D ReChord Semirigid Annuloplasty Ring; Memo 4D Semirigid Annuloplasty RingKRH2023-04-07
247761637250108K210006MI DeTACHDXC2021-03-04
247761477965754K180411MEMO 4DKRH2018-03-16
247762051495830K142221MEMO 3D ReChordKRH2014-08-29
247761692406460K023185ANNULOFLEX ANNUOPLASTY SYSTEM, MODEL AF 800KRH2002-12-17
247761092013337K021051ANNULOFLO SYSTEM, MITRAL MODEL AR700KRH2002-04-23
692691540236395
692691849122667
247761158855761
247761273598796
692691458025222
247761744467071
692691884629538
247762014115385
247762042769387

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KRH62026-04-14
LWR22016-01-08
DXC12021-03-04
MOP11995-06-20
LWQ11993-09-29