Baird Medical announced today that it submitted its disposable microwave ablation (MWA) needle system to the FDA for 510(k) clearance.
Guangzhou, China-based Baird submitted the system in search of an indication for the treatment of soft tissue microwave ablation. The FDA’s Center for Devices and Radiologic Health (CDRH) accepted the submission last month. Baird’s system already holds approval from China’s National Medical Products Administration, having earned that last month.
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