FDA 510(k) Applications Submitted by LAURENCE BIGIO

FDA 510(k) Number Submission Date Device Name Applicant
K080124 01/17/2008 VENTRI 1.1 GE MEDICAL SYSTEMS F.I. HAIFA
K083504 11/26/2008 GE DISCOVERY NM/CT 570C GE MEDICAL SYSTEMS F.I. HAIFA
K043381 12/09/2004 INFINIA LIGHTSPEED GE MEDICAL SYSTEMS F.I. HAIFA
K033874 12/15/2003 MYOLIGHT GE MEDICAL SYSTEMS F.I. HAIFA


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