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FDA 510(k) Applications Submitted by BRIAN ROTHMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110118
01/18/2011
STIMTRODE SINGLE USE NERVE STIMULATOR
XAVANT TECHNOLOGY (PTY), LTD.
K093591
11/19/2009
STIMPOD MODEL NMS-400 NERVE STIMULATOR
XAVANT TECHNOLOGY (PTY), LTD.
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