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THREE STAGE VENOUS RETURN CANNULA, MODEL 816460

Page Type
Cleared 510(K)
510(k) Number
K080034
510(k) Type
Traditional
Applicant
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
162 days
Submission Type
Summary

THREE STAGE VENOUS RETURN CANNULA, MODEL 816460

Page Type
Cleared 510(K)
510(k) Number
K080034
510(k) Type
Traditional
Applicant
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
162 days
Submission Type
Summary