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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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