FDA.reportPublic FDA data

WIDE USA CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30133974993013397499WIDE USA CORPORATION1Y2020-04-252210 E Winston Rd Anaheim CA US 92806

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2026341976137581K170783CX50N(CX50YQS)PGY2017-03-31
2026342023195298K170781MX50N(MX50YQS)PGY2017-04-04
2026341243944434K160355CX20N(CX20PUX)PGY2016-04-07
2026341045723197K160354MX50T(MX50TQS)PGY2016-05-02
2026341650874763K160353MX50N(MX50YQS)PGY2016-04-22
2026341176003077K160351CX50N, CX50YQSPGY2016-04-07
2026341050323862K160348CX30N (CX30PQX)PGY2016-04-14
2026341895720515K160346MX30N(MX30TQS)PGY2016-04-14
2026341279058421K110596MW100 (MAMMOGRAPHY) LCD MONITOR SYSTEMLLZ2011-11-18
2026341582935588K052312WIDE 5MP (MAMMO) LCD MONITOR SYSTEMLLZ2005-10-07
2026341721119565K032960WIDE 2MP TFT LCD MONITOR SYSTEM IF 1902ALLZ2003-10-08
2026341766317914K032174WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103ALLZ2003-07-24
2026341167477633K0319295MP TFT LCD MONITOR SYSTEM IF2105A BY WIDE CORPORATIONLLZ2003-07-08

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PGY82017-04-04
LLZ52011-11-18