Last synced on 29 August 2025 at 11:05 pm

SAFE MAXI VENOUS/CARDIOTOMY RESERVIOR, MODEL 016045

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022281
510(k) Type
Traditional
Applicant
POLYSTAN A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
8/6/2002
Days to Decision
22 days
Submission Type
Summary

SAFE MAXI VENOUS/CARDIOTOMY RESERVIOR, MODEL 016045

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022281
510(k) Type
Traditional
Applicant
POLYSTAN A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
8/6/2002
Days to Decision
22 days
Submission Type
Summary