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IMPELLA 5.0 CATHETER FAMILY

Page Type
Cleared 510(K)
510(k) Number
K083111
510(k) Type
Traditional
Applicant
ABIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2009
Days to Decision
177 days
Submission Type
Summary

IMPELLA 5.0 CATHETER FAMILY

Page Type
Cleared 510(K)
510(k) Number
K083111
510(k) Type
Traditional
Applicant
ABIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2009
Days to Decision
177 days
Submission Type
Summary