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PVS 1400 GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K990823
510(k) Type
Traditional
Applicant
PRECISION VASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1999
Days to Decision
133 days
Submission Type
Summary

PVS 1400 GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K990823
510(k) Type
Traditional
Applicant
PRECISION VASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/1999
Days to Decision
133 days
Submission Type
Summary