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QUADROX-I MICROPORPOROUS MEMBRANE OXGENATOR SERIES AND QUDROX-ID DIFFUSION MEMBRANE OXYGENATORS SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112360
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
29 days
Submission Type
Summary

QUADROX-I MICROPORPOROUS MEMBRANE OXGENATOR SERIES AND QUDROX-ID DIFFUSION MEMBRANE OXYGENATORS SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112360
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/15/2011
Days to Decision
29 days
Submission Type
Summary