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COBE OPTIMA AND COBE CML DUO MEMBRANE OXYGENATORS

Page Type
Cleared 510(K)
510(k) Number
K964043
510(k) Type
Traditional
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1997
Days to Decision
355 days
Submission Type
Summary

COBE OPTIMA AND COBE CML DUO MEMBRANE OXYGENATORS

Page Type
Cleared 510(K)
510(k) Number
K964043
510(k) Type
Traditional
Applicant
COBE CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1997
Days to Decision
355 days
Submission Type
Summary