Last synced on 14 November 2025 at 11:06 pm

PVS 1300 NEURO GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K002907
510(k) Type
Traditional
Applicant
PRECISION VASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2001
Days to Decision
171 days
Submission Type
Summary

PVS 1300 NEURO GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K002907
510(k) Type
Traditional
Applicant
PRECISION VASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2001
Days to Decision
171 days
Submission Type
Summary