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COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

Page Type
Cleared 510(K)
510(k) Number
K013480
510(k) Type
Special
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
28 days
Submission Type
Summary

COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

Page Type
Cleared 510(K)
510(k) Number
K013480
510(k) Type
Special
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
28 days
Submission Type
Summary