DATASCOPE FIBER OPTIC PRESSURE SENSOR INTRA-AORTIC BALLOON CATHETER AND CS300 INTRA-AORTIC BALLOON PUMP CONTROL SYSTEM— 510(k) K063525

Substantially Equivalent

Datascope Corp.

FDA 510(k) clearance K063525 for DATASCOPE FIBER OPTIC PRESSURE SENSOR INTRA-AORTIC BALLOON CATHETER AND CS300 INTRA-AORTIC BALLOON PUMP CONTROL SYSTEM, Substantially Equivalent on 2007-01-05. Applicant: Datascope Corp..

Clearance details

Applicant: Datascope Corp.
Product code: Code DSP
Advisory panel: Cardiovascular
Date received: 2006-11-22
Decision date: 2007-01-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Fairfield, NJ, US

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Adverse events under product code DSP

product code DSP

Death: 317
Injury: 566
Malfunction: 36,831
Other: 4
Total: 37,718

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.