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AORTIC ROOT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K790565
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1979
Days to Decision
84 days

AORTIC ROOT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K790565
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1979
Days to Decision
84 days