FDA.reportPublic FDA data

SPIRACLE TECHNOLOGY

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
20307453000204983SPIRACLE TECHNOLOGY1N2026-01-0110601 Calle Lee Ste 190 Los Alamitos CA US 90720

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
523991466682669K963755SPIRACLE TECHNOLOGY - MODEL 302 OX INHALATORCBP1997-04-08
523991036778018K953349SPIRACLE TECHNOLOTY GASEOUS OXYGEN SUPPLY VALVECBP1996-02-29
523991380537122K171961Compower CPR Mask With Oxygen Port, Compower CPR Mask Without Oxygen Port, Compower Infant CPR Mask, Compower Non-Rebreathing Valve (22mm/15mmOD), Non-Rebreathing Valve (22mm/18.5mm)CBP2017-11-17
523991395877368K070371FINGERTIP PULSE OXIMETER MD300CDQA2007-08-13
523991283195893K043286ANEROID SPHYGMOMANOMETER, MODEL BK2002DXQ2005-01-13
523991012274597K031434BAWMED E-Z BAG RESUSCITATORBTM2004-02-06
523991053487803
523991134052113
523991161385063
523991404874959
523991451402315

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
CBP32017-11-17
DQA12007-08-13
DXQ12005-01-13
BTM12004-02-06

PMN#

GUDID#