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HEARTPORT ENDOARTERIAL RETURN CANNUAL

Page Type
Cleared 510(K)
510(k) Number
K955121
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1996
Days to Decision
183 days
Submission Type
Summary

HEARTPORT ENDOARTERIAL RETURN CANNUAL

Page Type
Cleared 510(K)
510(k) Number
K955121
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1996
Days to Decision
183 days
Submission Type
Summary