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CARDIOCASSETTE II, AMBULATORY ECG SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790509
510(k) Type
Traditional
Applicant
CAMBRIDGE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1979
Days to Decision
8 days

CARDIOCASSETTE II, AMBULATORY ECG SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790509
510(k) Type
Traditional
Applicant
CAMBRIDGE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1979
Days to Decision
8 days