FDA.reportPublic FDA data

Alyssa Haig

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30057784583005778458Alyssa Haig1N2026-01-01150 Verona St ROCHESTER NY US 14608

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
678311259804588K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorKPR2026-01-20
678311166155389K192512Focus 35C Detector, Trimax 35C DetectorMQB2019-10-16
678311096915286K120246KODAK DIRECTVIEW CR MAMMOGRAPHY SYSTEM (USING CARESTREAM CR MAMMOGRAPHY CASSETTE WITH SNP-M1 SCREEN)MUE2012-08-28
678311813101895K100094CARESTREAM IMAGE SUITELLZ2010-03-11
678311406693184K011486Q-RAD RADIOGRAPHIC SYSTEMKPR2001-06-20
678311005438946
678311475189336
678311741878697
678311977295742
678312039914184

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KPR22026-01-20
MQB12019-10-16
MUE12012-08-28
LLZ12010-03-11