PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)

PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040) is an FDA 510(k)-cleared medical device (K990960) manufactured by Perimed, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 22, 1999. Regulation: 8.