Zhejiang Lude Technology Development Co., Ltd.

Zhejiang Lude Technology Development Co., Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2022.

Top product codes for Zhejiang Lude Technology Development Co., Ltd.

DXQ — Cardiovascular1 device

Recent clearances by Zhejiang Lude Technology Development Co., Ltd.

K221857 — Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201Code DXQ·2022-10-13

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