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CARDIOLINE AR 600, AR 1200, AR 2100

Page Type
Cleared 510(K)
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)
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