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Spectre guidewire

Page Type
Cleared 510(K)
510(k) Number
K163444
510(k) Type
Special
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2017
Days to Decision
29 days
Submission Type
Summary

Spectre guidewire

Page Type
Cleared 510(K)
510(k) Number
K163444
510(k) Type
Special
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2017
Days to Decision
29 days
Submission Type
Summary