Last synced on 9 May 2025 at 11:05 pm

PureFlex Arterial Cannulae

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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