FDA 510(k) Applications Submitted by Veronica A. 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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