K020529

Substantially Equivalent

LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2

Applicant: A-Med Systems, Inc.
Product code: KFM
Advisory panel: Cardiovascular
Date received: 2002-02-19
Decision date: 2002-08-26
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, 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.