Zhejiang Lude Technology Development Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Zhejiang Lude Technology Development Co., Ltd. - FDA 510(k) Cleared D...
Recent clearances: Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201
1
Total
1
Cleared
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Denied
Zhejiang Lude Technology Development Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wenzhou, CN.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zhejiang Lude Technology Development Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zhejiang Lude Technology Development Co., Ltd.
1 devices