Last synced on 25 January 2026 at 3:41 am

PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050447
510(k) Type
Special
Applicant
Dideco S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2005
Days to Decision
14 days
Submission Type
Summary

PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050447
510(k) Type
Special
Applicant
Dideco S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2005
Days to Decision
14 days
Submission Type
Summary