Last synced on 14 November 2025 at 11:06 pm

ROTATING HEMOSTATIC VALVE

Page Type
Cleared 510(K)
510(k) Number
K883916
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1988
Days to Decision
42 days

ROTATING HEMOSTATIC VALVE

Page Type
Cleared 510(K)
510(k) Number
K883916
510(k) Type
Traditional
Applicant
DEVICES FOR VASCULAR INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1988
Days to Decision
42 days