Infrared Thermometer (Model: LX-26E, LX-260TE, PRO LX-261E, LX-360, LX-361T, BW-CX10)— 510(k) K160816

Substantially Equivalent

Nexmed Technology Co., Ltd.

FDA 510(k) clearance K160816 for Infrared Thermometer (Model: LX-26E, LX-260TE, PRO LX-261E, LX-360, LX-361T, BW-CX10), Substantially Equivalent on 2016-09-21. Applicant: Nexmed Technology Co., Ltd..

Clearance details

Applicant: Nexmed Technology Co., Ltd.
Product code: Code FLL
Advisory panel: General Hospital
Date received: 2016-03-24
Decision date: 2016-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code FLL

product code FLL

Death: 3
Malfunction: 557
Total: 560

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.