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SHILEY FEMORAL CANNULAE INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K881073
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1988
Days to Decision
87 days

SHILEY FEMORAL CANNULAE INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K881073
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/1988
Days to Decision
87 days