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HEARTVIEW(R) CORONARY ANGIOGRAPH DIAGRAM/REPORT SY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932410
510(k) Type
Traditional
Applicant
HEARTWARE INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1993
Days to Decision
209 days
Submission Type
Statement

HEARTVIEW(R) CORONARY ANGIOGRAPH DIAGRAM/REPORT SY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932410
510(k) Type
Traditional
Applicant
HEARTWARE INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1993
Days to Decision
209 days
Submission Type
Statement