Last synced on 14 November 2025 at 11:06 pm

VASCULAR OCCLUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983483
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1999
Days to Decision
170 days
Submission Type
Summary

VASCULAR OCCLUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983483
510(k) Type
Traditional
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1999
Days to Decision
170 days
Submission Type
Summary