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CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902493
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/6/1990
Days to Decision
31 days

CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902493
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/6/1990
Days to Decision
31 days