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CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

Page Type
Cleared 510(K)
510(k) Number
K071572
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2007
Days to Decision
45 days
Submission Type
Summary

CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

Page Type
Cleared 510(K)
510(k) Number
K071572
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2007
Days to Decision
45 days
Submission Type
Summary