Linshom Announces FDA Clearance of the Linshom Respiratory Monitoring Device (LRMD)
Source: External source
Linshom announced today U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s first product, a small, non-invasive respiratory monitor that addresses the growing need for continuous respiratory monitoring for patients susceptible to respiratory depression and compromise.
Posted February 3, 2020
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