Last synced on 12 October 2025 at 8:21 pm

VANTAGE DIALTAION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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