FDA 510(k) Applications Submitted by MARK WATSON

FDA 510(k) Number Submission Date Device Name Applicant
K080820 03/24/2008 TEM 3002G- HN DUAL TUNE HEAD COIL MR INSTRUMENTS, INC.
K052200 08/12/2005 TEM 3000 HEAD COIL MR INSTRUMENTS INC.
K072931 10/16/2007 MC 3003G-32R HEAD COIL MR INSTRUMENTS, INC.


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