LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2— 510(k) K020529
Substantially EquivalentA-Med Systems, Inc.
FDA 510(k) clearance K020529 for LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2, Substantially Equivalent on 2002-08-26. Applicant: A-Med Systems, Inc..
Clearance details
- Applicant
- A-Med Systems, Inc.
- Product code
- Code KFM
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Sacramento, CA, US
Adverse events under product code KFM
product code KFM- Death
- 109
- Injury
- 241
- Malfunction
- 1,779
- Total
- 2,129
Source: openFDA MAUDE database, through . 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.