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MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K971105
510(k) Type
Traditional
Applicant
AVECOR CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1997
Days to Decision
107 days
Submission Type
Summary

MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K971105
510(k) Type
Traditional
Applicant
AVECOR CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1997
Days to Decision
107 days
Submission Type
Summary