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CARDIAC PERFORMANCE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864583
510(k) Type
Traditional
Applicant
VASCULAR TECHNOLOGY INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1987
Days to Decision
172 days

CARDIAC PERFORMANCE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864583
510(k) Type
Traditional
Applicant
VASCULAR TECHNOLOGY INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1987
Days to Decision
172 days