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CARDIOSAVE Hybrid and Rescue Intra-Aortic Balloon Pump, CARDIOSAVE Li-Ion Battery Transport and Storage Case

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163542
510(k) Type
Special
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
46 days
Submission Type
Summary

CARDIOSAVE Hybrid and Rescue Intra-Aortic Balloon Pump, CARDIOSAVE Li-Ion Battery Transport and Storage Case

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163542
510(k) Type
Special
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
46 days
Submission Type
Summary