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VIRTUOSAPH

Page Type
Cleared 510(K)
510(k) Number
K031891
510(k) Type
Traditional
Applicant
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2003
Days to Decision
46 days
Submission Type
Summary

VIRTUOSAPH

Page Type
Cleared 510(K)
510(k) Number
K031891
510(k) Type
Traditional
Applicant
TERUMO CARDIOVASCULAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2003
Days to Decision
46 days
Submission Type
Summary