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INTRAVASCULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K812159
510(k) Type
Traditional
Applicant
PIONEER VIGGO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1981
Days to Decision
33 days

INTRAVASCULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K812159
510(k) Type
Traditional
Applicant
PIONEER VIGGO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1981
Days to Decision
33 days