FDA.reportPublic FDA data

SENTREHEART INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30058022383006482885SENTREHEART INC.1N2020-04-25300 Saginaw Dr Redwood City CA US 94063

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2350391234687945K153096LARIAT RS Suture Delivery DeviceGAT2015-11-25
2350391428898645K142241LARIAT sulture Delivery DeviceGAT2014-09-12
2350392055779782K090385LARIAT II SUTURE DELIVERY DEVICEGAT2009-05-06
2350391544752783K080364FINDRWIRZ GUIDE WIRE SYSTEMDQX2008-08-11
2350391738849252K070126OCCLUSION BALLOON CATHETERDQY2008-02-08
2350391356122521
2350391651111601

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GAT32015-11-25
DQX12008-08-11
DQY12008-02-08

PMN#