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PureFlex Arterial Cannulae

Page Type
Cleared 510(K)
510(k) Number
K180979
510(k) Type
Traditional
Applicant
Sorin Group Italia S.r.l
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/16/2018
Days to Decision
217 days
Submission Type
Summary

PureFlex Arterial Cannulae

Page Type
Cleared 510(K)
510(k) Number
K180979
510(k) Type
Traditional
Applicant
Sorin Group Italia S.r.l
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
11/16/2018
Days to Decision
217 days
Submission Type
Summary