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GUIDELINER CATHETER, MODELS 5571, 5572, 5573

Page Type
Cleared 510(K)
510(k) Number
K091750
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2009
Days to Decision
141 days
Submission Type
Summary

GUIDELINER CATHETER, MODELS 5571, 5572, 5573

Page Type
Cleared 510(K)
510(k) Number
K091750
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/2009
Days to Decision
141 days
Submission Type
Summary