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CARDIOHELP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102726
510(k) Type
Traditional
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/4/2011
Days to Decision
195 days
Submission Type
Summary

CARDIOHELP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102726
510(k) Type
Traditional
Applicant
MAQUET CARDIOPULMONARY AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/4/2011
Days to Decision
195 days
Submission Type
Summary