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VERIPATH PERIPHERAL GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K994229
510(k) Type
Special
Applicant
Advanced Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2000
Days to Decision
71 days
Submission Type
Summary

VERIPATH PERIPHERAL GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K994229
510(k) Type
Special
Applicant
Advanced Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2000
Days to Decision
71 days
Submission Type
Summary