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CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR AND ARTERIAL FILTER

Page Type
Cleared 510(K)
510(k) Number
K071494
510(k) Type
Traditional
Applicant
Terumo Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2007
Days to Decision
47 days
Submission Type
Summary

CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR AND ARTERIAL FILTER

Page Type
Cleared 510(K)
510(k) Number
K071494
510(k) Type
Traditional
Applicant
Terumo Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2007
Days to Decision
47 days
Submission Type
Summary