Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17

Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 is an FDA 510(k)-cleared medical device (K221616) manufactured by Caf Medical Solutions, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 2022. Regulation: 8.