Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors

Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors is an FDA 510(k)-cleared medical device (K181738) manufactured by Surgical Instrument Service and Savings Inc (Dba Medline. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 21, 2019. Regulation: 8.