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D903 AVANT ADULT HOLLOW FIBER OXYGENATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980600
510(k) Type
Traditional
Applicant
DIDECO S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1998
Days to Decision
176 days
Submission Type
Summary

D903 AVANT ADULT HOLLOW FIBER OXYGENATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980600
510(k) Type
Traditional
Applicant
DIDECO S.P.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1998
Days to Decision
176 days
Submission Type
Summary