GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR— 510(k) K043352

Substantially Equivalent

Gocanning Technology , Ltd.

FDA 510(k) clearance K043352 for GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR, Substantially Equivalent on 2005-03-31. Applicant: Gocanning Technology , Ltd..

Clearance details

Applicant: Gocanning Technology , Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2004-12-06
Decision date: 2005-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flagstaff, AZ, US

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.