Last synced on 14 November 2025 at 11:06 pm

Aortic Arch Cannulae, Optiflow Aortic Arch Cannulae

Page Type
Cleared 510(K)
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)
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