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DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010478
510(k) Type
Abbreviated
Applicant
DIDECO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2001
Days to Decision
219 days
Submission Type
Summary

DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010478
510(k) Type
Abbreviated
Applicant
DIDECO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2001
Days to Decision
219 days
Submission Type
Summary