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QUICKDRAW VENOUS CANNULA

Page Type
Cleared 510(K)
510(k) Number
K981995
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1999
Days to Decision
316 days
Submission Type
Summary

QUICKDRAW VENOUS CANNULA

Page Type
Cleared 510(K)
510(k) Number
K981995
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1999
Days to Decision
316 days
Submission Type
Summary