FDA.reportPublic FDA data

KITRON AB

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30098340763009834076KITRON AB1N2026-01-01Mobelvagen 5 Jonkoping SE SE-55652

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1492881717191738P150046NEVISENSEONV2017-06-28
1492881417627985K133565LEKSELL GAMMA KNIFE PERFEXIONIWB2014-05-09
1492881266696185K092868CELLAVISION DM1200 AUTOMATED HEMATOLOGY ANALYZER, MODEL XU-10127JOY2009-11-20
1492881053688697K033840CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZERJOY2004-02-10
1492881172152258K023354COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EBTI2003-09-05
1492881008175876
1492881172152258
1492881266696185

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
JOY22009-11-20
ONV12017-06-28
IWB12014-05-09
BTI12003-09-05