FDA 510(k) Applications Submitted by MARY E BEST

FDA 510(k) Number Submission Date Device Name Applicant
K013963 12/03/2001 MODEL 9210 DELIVERY CATHETER, MODEL 9210 MEDTRONIC VASCULAR
K022238 07/11/2002 MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626 MEDTRONIC VASCULAR
K953567 07/31/1995 INCSTAR 25-HYDROXYVITMIN D 1251 RIA INCSTAR CORP.


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