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ADDITIONAL LETTER DESIGNATION FOR AORTIC ARCH CAN.

Page Type
Cleared 510(K)
510(k) Number
K870826
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1987
Days to Decision
20 days

ADDITIONAL LETTER DESIGNATION FOR AORTIC ARCH CAN.

Page Type
Cleared 510(K)
510(k) Number
K870826
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1987
Days to Decision
20 days