Zhejiang Lude Technology Development Co., Ltd. - FDA 510(k) Cleared D...
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.
1 devices