Linshom Respiratory Monitoring Device (LRMD)

Linshom Respiratory Monitoring Device (LRMD) is an FDA 510(k)-cleared medical device (K190734) manufactured by Linshom Management, LLC. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 2020. Regulation: 8.