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DIRECTFLOW ARTERIAL CANNULA

Page Type
Cleared 510(K)
510(k) Number
K990772
510(k) Type
Special
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1999
Days to Decision
14 days
Submission Type
Summary

DIRECTFLOW ARTERIAL CANNULA

Page Type
Cleared 510(K)
510(k) Number
K990772
510(k) Type
Special
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1999
Days to Decision
14 days
Submission Type
Summary