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HEARTPORT ENDOARTERIAL RETURN CANNULA

Page Type
Cleared 510(K)
510(k) Number
K971291
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1997
Days to Decision
71 days
Submission Type
Summary

HEARTPORT ENDOARTERIAL RETURN CANNULA

Page Type
Cleared 510(K)
510(k) Number
K971291
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1997
Days to Decision
71 days
Submission Type
Summary