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MODIFIED ANGIOGRAPHIC INJECTOR AND SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K902221
510(k) Type
Traditional
Applicant
MALLINCKRODT GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1990
Days to Decision
83 days

MODIFIED ANGIOGRAPHIC INJECTOR AND SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K902221
510(k) Type
Traditional
Applicant
MALLINCKRODT GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1990
Days to Decision
83 days