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CARDIOLINE AR 600, AR 1200, AR 2100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051534
510(k) Type
Special
Applicant
ET MEDICAL DEVICES SPA
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/5/2005
Days to Decision
117 days
Submission Type
Summary

CARDIOLINE AR 600, AR 1200, AR 2100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051534
510(k) Type
Special
Applicant
ET MEDICAL DEVICES SPA
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/5/2005
Days to Decision
117 days
Submission Type
Summary