FDA.reportPublic FDA data

Response Biomedical Corp.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30042056923004205692Response Biomedical Corp.1N2026-01-011781-75th Avenue W. Vancouver British Columbia CA V6P 6P2

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
200651628442323K110534RANDOX LIQUID CARDIAC CONTROL LEVELS 1, 2 AND 3JJY2012-01-23
200651395408227K091235RAMP RSV ASSAYGQG2009-07-24
200651633444475K080973CLINIQA LIQUID QC COMPLETE CARDIAC MARKER CONTROL, LEVELS 1,2, AND 3; CARDIAC MARKER CONTROL-LOW, AND LINICAL CARDIACJJY2008-06-02
200651769616701K063662RAMP NT-PROBNP ASSAYNBC2008-07-21
200651393999867K033747RAMP CK-MB ASSAYJHX2004-05-17
200651355858082K033745RAMP TROPONIN I ASSAYMMI2004-05-17
200651405294668K012040RAMP MYOGLOBIN ASSAYDDR2001-12-18
200651019567628

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
JJY22012-01-23
GQG12009-07-24
NBC12008-07-21
JHX12004-05-17
MMI12004-05-17
DDR12001-12-18

PMN#