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DATASCOPE FIBER OPTIC PRESSURE SENSOR INTRA-AORTIC BALLOON CATHETER AND CS300 INTRA-AORTIC BALLOON PUMP CONTROL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063525
510(k) Type
Special
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2007
Days to Decision
44 days
Submission Type
Summary

DATASCOPE FIBER OPTIC PRESSURE SENSOR INTRA-AORTIC BALLOON CATHETER AND CS300 INTRA-AORTIC BALLOON PUMP CONTROL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063525
510(k) Type
Special
Applicant
Datascope Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2007
Days to Decision
44 days
Submission Type
Summary