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MK5 DETECTOR & ALARM, ARRHYTHMIA W/SOFTWARE 2.11

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900607
510(k) Type
Traditional
Applicant
CARDIODATA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1990
Days to Decision
250 days

MK5 DETECTOR & ALARM, ARRHYTHMIA W/SOFTWARE 2.11

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900607
510(k) Type
Traditional
Applicant
CARDIODATA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1990
Days to Decision
250 days