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FDA 510(k) Applications Submitted by Jennifer Rautine
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160198
01/28/2016
UreTron MultiProbe Lithotripter System
Med-Sonics Corp
K162119
08/01/2016
UreTron PF Series Probe
MED-SONICS CORP.
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