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VANTAGE DIALTAION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K934433
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1993
Days to Decision
87 days
Submission Type
Summary

VANTAGE DIALTAION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K934433
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1993
Days to Decision
87 days
Submission Type
Summary