FDA 510(k) Applications Submitted by E. JOSEPH MCMULLEN

FDA 510(k) Number Submission Date Device Name Applicant
K981722 05/15/1998 QUIDEL HOME PREGNANCY TEST QUIDEL CORP.
K003395 11/01/2000 GEN-PROBE APTIMA COMBO 2 ASSAY GEN-PROBE, INC.
K063451 11/15/2006 GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1199 GEN-PROBE, INC.
K083430 11/19/2008 REAL-TIME PCR INTERNAL CONTROL 2B SET NANOGEN, INC.
K063664 12/08/2006 GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091 GEN-PROBE, INC.


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