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PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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