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HEARTCARD CARDIAC EVENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944362
510(k) Type
Traditional
Applicant
INSTROMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1995
Days to Decision
365 days
Submission Type
Statement

HEARTCARD CARDIAC EVENT MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944362
510(k) Type
Traditional
Applicant
INSTROMEDIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1995
Days to Decision
365 days
Submission Type
Statement