preCARDIA Occlusion System— 510(k) K221294

Unknown

Abiomed, Inc.

FDA 510(k) clearance K221294 for preCARDIA Occlusion System, Unknown on 2023-06-30. Applicant: Abiomed, Inc..

Clearance details

Applicant: Abiomed, Inc.
Product code: Code MJN
Advisory panel: Cardiovascular
Date received: 2022-05-04
Decision date: 2023-06-30
Decision: Unknown
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MJN

product code MJN

Death: 31
Injury: 240
Malfunction: 827
Total: 1,098

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.