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FDA 510(k) Applications Submitted by KRISTY K MOLLNER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991991
06/14/1999
DUPEL IONTOPHORESIS SYSTEM
EMPI
K013517
10/22/2001
10600 DEFLECTABLE CATHETER SYSTEM, MODEL 10600
MEDTRONIC VASCULAR
K033989
12/23/2003
MEDTRONIC SELECTSITE DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59 AND C304-L69
MEDTRONIC INC. CARDIAC RHYTHM MANAGEMENT
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