FDA.reportPublic FDA data

JOHN ROSS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30083041803008164200JOHN ROSS1N2026-01-0135768 West Santa Monica Avenue Maricopa AZ US 85138

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1256821483859521K211108Prudent 1717, Prudent 1417, Prudent 1212MQB2021-06-04
1256821698106566K190691Pixx2430 Digital Diagnostic X-Ray Receptor PanelMQB2019-04-04
1256821893200384K182533PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor PanelsMQB2018-10-04
1256821066823142K180976PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor PanelsMQB2018-05-24
1256822013064406K152151ATAL 9MQB2015-11-10
1256821828740515K113812ATAL-8MQB2012-05-03
1256821734971920K110040OMNIVISIONLLZ2011-01-26

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQB62021-06-04
LLZ12011-01-26