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PROTEK Duo 31 Fr. Veno-Venous Cannula Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160257
510(k) Type
Special
Applicant
CARDIAC ASSIST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2016
Days to Decision
32 days
Submission Type
Summary

PROTEK Duo 31 Fr. Veno-Venous Cannula Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160257
510(k) Type
Special
Applicant
CARDIAC ASSIST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2016
Days to Decision
32 days
Submission Type
Summary