Last synced on 12 September 2025 at 11:05 pm

HEARTVIEW(R) CORONARY ANGIOGRAPH DIAGRAM/REPORT SY

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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