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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