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ANGEION HEMOSTASIS VALVE INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K894446
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1989
Days to Decision
136 days

ANGEION HEMOSTASIS VALVE INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K894446
510(k) Type
Traditional
Applicant
ANGEION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1989
Days to Decision
136 days