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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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