FDA.reportPublic FDA data

LI QIAN

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30144560663014456066LI QIAN1N2026-01-011120 Alpha Dr Alpharetta GA US 30004

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2188481197935354K181508U&U Blood Collection SetsFMI2019-02-13
2188481644077701K160855U&U Enteral SyringePNR2016-11-22
2188481681146113K152808U&U Insulin Syringe with/without Safety Retractable DeviceMEG2016-03-25
2188481404121594K151151U & U Intravascular Administration SetFPA2015-09-24
2188481211512591K143637U&U Sterilization Pouch and RollFRG2015-09-09
2188481129286091K142765TM SAFETY NEEDLEFMI2015-08-11
2188481521884072K132553U&U STERILE PISTON SYRINGE WITHOUT NEEDLEFMF2014-02-27
2188481698493583K132552U&U STERILE HYPODERMIC NEEDLEFMI2013-11-13
2188481854003924K131954MEDI PEN NEEDLEFMI2014-05-29
2188481336281266
2188481507878538
2188481885498219
2188481955439951
2188481180027051
2188481431967765
2188481462019852
2188481518050252
2188481957954396

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FMI42019-02-13
PNR12016-11-22
MEG12016-03-25
FPA12015-09-24
FRG12015-09-09
FMF12014-02-27