FDA 510(k) Applications Submitted by NEOCOIL

FDA 510(k) Number Submission Date Device Name Applicant
K070778 03/21/2007 NEOCOIL 3.0T 6-CHANNEL CAROTID ARRAY COIL NEOCOIL
K071311 05/09/2007 NEOCOIL 1.5T 8-CHANNEL SHOULDER ARRAY COIL NEOCOIL
K071611 06/13/2007 NEOCOIL 3.0T 8-CHANNEL SHOULDER ARRAY COIL NEOCOIL
K073236 11/16/2007 NEOCOIL 3.0T 32-CHANNEL TORSO ARRAY COIL FOR GE NEOCOIL


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