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IMAGEVIEW CORONARY ANGIOGRAPHY DISPLAY AND REVIEW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K972229
510(k) Type
Traditional
Applicant
HEARTWARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1997
Days to Decision
125 days
Submission Type
Summary

IMAGEVIEW CORONARY ANGIOGRAPHY DISPLAY AND REVIEW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K972229
510(k) Type
Traditional
Applicant
HEARTWARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1997
Days to Decision
125 days
Submission Type
Summary