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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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