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IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063723
510(k) Type
Traditional
Applicant
ABIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2008
Days to Decision
532 days
Submission Type
Summary

IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063723
510(k) Type
Traditional
Applicant
ABIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2008
Days to Decision
532 days
Submission Type
Summary