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MODIFIED SHILEY DUAL LUMEN SUBCLAVIAN CANNULA

Page Type
Cleared 510(K)
510(k) Number
K881290
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/1988
Days to Decision
30 days

MODIFIED SHILEY DUAL LUMEN SUBCLAVIAN CANNULA

Page Type
Cleared 510(K)
510(k) Number
K881290
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/1988
Days to Decision
30 days