SUNPEX TECHNOLOGIES MODEL PW— 510(k) K024175

Substantially Equivalent

Sunpex Technology Co., Ltd.

FDA 510(k) clearance K024175 for SUNPEX TECHNOLOGIES MODEL PW, Substantially Equivalent on 2003-05-01. Applicant: Sunpex Technology Co., Ltd..

Clearance details

Applicant: Sunpex Technology Co., Ltd.
Product code: Code ITI
Advisory panel: Physical Medicine
Date received: 2002-12-18
Decision date: 2003-05-01
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Baltimore, MD, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

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.