GREENLIGHT 300— 510(k) K040410

Substantially Equivalent

A C Cossor & Son (Surgical) Limited

FDA 510(k) clearance K040410 for GREENLIGHT 300, Substantially Equivalent on 2004-05-05. Applicant: A C Cossor & Son (Surgical) Limited.

Clearance details

Applicant: A C Cossor & Son (Surgical) Limited
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2004-02-18
Decision date: 2004-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.