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PROWLER PLUS INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K993266
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1999
Days to Decision
28 days
Submission Type
Summary

PROWLER PLUS INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K993266
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1999
Days to Decision
28 days
Submission Type
Summary