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FDA 510(k) Applications Submitted by DAVID M PETERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090267
02/03/2009
SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64
MIDWEST R.F. LLC.
K051618
06/17/2005
SPECIAL PROCEDURES II HEAD COIL, MODEL 1400GE-64
MIDWEST R.F. LLC.
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