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QUADROX-IR ADULT AND SMALL ADULT

Page Type
Cleared 510(K)
510(k) Number
K133265
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2013
Days to Decision
20 days
Submission Type
Summary

QUADROX-IR ADULT AND SMALL ADULT

Page Type
Cleared 510(K)
510(k) Number
K133265
510(k) Type
Special
Applicant
MAQUET CARDIOPULMONARY AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2013
Days to Decision
20 days
Submission Type
Summary