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HEARTPORT ENDOSINUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K961270
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1996
Days to Decision
77 days
Submission Type
Summary

HEARTPORT ENDOSINUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K961270
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1996
Days to Decision
77 days
Submission Type
Summary