Shenzhen Aeon Technology Co., Ltd.

Shenzhen Aeon Technology Co., Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2017, most recent 2020.

Top product codes for Shenzhen Aeon Technology Co., Ltd.

DQA — Cardiovascular2 devices
FLL — General Hospital1 device

Recent clearances by Shenzhen Aeon Technology Co., Ltd.

K200414 — Pulse OximeterCode DQA·2020-09-23
K190869 — Pulse OximeterCode DQA·2019-09-13
K171578 — Infrared thermometerCode FLL·2017-11-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.