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Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162215
510(k) Type
Traditional
Applicant
SORIN GROUP ITALIA S.R.L
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
6/16/2017
Days to Decision
312 days
Submission Type
Summary

Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162215
510(k) Type
Traditional
Applicant
SORIN GROUP ITALIA S.R.L
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
6/16/2017
Days to Decision
312 days
Submission Type
Summary