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ASI HEMOSTASIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901336
510(k) Type
Traditional
Applicant
ADVANCED SURGICAL INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1990
Days to Decision
90 days

ASI HEMOSTASIS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K901336
510(k) Type
Traditional
Applicant
ADVANCED SURGICAL INTERVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1990
Days to Decision
90 days