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FDA 510(k) Applications Submitted by Veronica Meridith
FDA 510(k) Number
Submission Date
Device Name
Applicant
K182590
09/20/2018
1.5T AIR MP M, 1.5T AIR MP L, 1.5T 16ch AIR AA, 1.5T 30ch AIR AA
GE Healthcare
K180666
03/14/2018
48CH Head Coil
GE Healthcare Coils (USA Instruments, Inc.)
K182504
09/12/2018
3.0T Air MP M, 3.0T Air MP L
GE Healthcare Coils (USA Instruments, Inc.)
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