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AORTIC ROOT CANNULA W/INTEGRAL PRESS

Page Type
Cleared 510(K)
510(k) Number
K831591
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
44 days

AORTIC ROOT CANNULA W/INTEGRAL PRESS

Page Type
Cleared 510(K)
510(k) Number
K831591
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
44 days