FDA 510(k) Applications Submitted by PRECISION VASCULAR SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K990823 03/12/1999 PVS 1400 GUIDEWIRE PRECISION VASCULAR SYSTEMS, INC.
K002707 08/30/2000 PVS 1400 GUIDE WITE WITH HYDROPHILIC COATING PRECISION VASCULAR SYSTEMS, INC.
K002907 09/18/2000 PVS 1300 NEURO GUIDE WIRE PRECISION VASCULAR SYSTEMS, INC.
K020733 03/06/2002 PVS 1500 SDS PRECISION VASCULAR SYSTEMS, INC.
K032146 07/14/2003 PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES PRECISION VASCULAR SYSTEMS, INC.
K032494 08/13/2003 PVS 1700 STEERABLE DELIVERY SYSTEM MICROCATHETER PRECISION VASCULAR SYSTEMS, INC.
K023700 11/04/2002 PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE PRECISION VASCULAR SYSTEMS, INC.


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