Last synced on 14 November 2025 at 11:06 pm

5F ENVOY(TM) GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K945705
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1995
Days to Decision
87 days
Submission Type
Summary

5F ENVOY(TM) GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K945705
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1995
Days to Decision
87 days
Submission Type
Summary