EPICARDIA 5000— 510(k) K090834

Substantially Equivalent

Medicomp, Inc.

FDA 510(k) clearance K090834 for EPICARDIA 5000, Substantially Equivalent on 2009-05-15. Applicant: Medicomp, Inc..

Clearance details

Applicant: Medicomp, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 2009-03-27
Decision date: 2009-05-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

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.