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CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862375
510(k) Type
Traditional
Applicant
GRANDCOR MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1986
Days to Decision
7 days

CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862375
510(k) Type
Traditional
Applicant
GRANDCOR MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1986
Days to Decision
7 days