Last synced on 25 January 2026 at 3:41 am

CARDIOCAP CMX-104 MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903237
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
359 days

CARDIOCAP CMX-104 MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903237
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
359 days