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HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K974736
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1998
Days to Decision
208 days
Submission Type
Summary

HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K974736
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1998
Days to Decision
208 days
Submission Type
Summary