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CARDIOCAP DR-124 RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910620
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/7/1991
Days to Decision
84 days

CARDIOCAP DR-124 RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910620
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/7/1991
Days to Decision
84 days