FREEDOM OXIMETER/EEG DIGITAL INTERFACE

FREEDOM OXIMETER/EEG DIGITAL INTERFACE is an FDA 510(k)-cleared medical device (K924752) manufactured by Pro-Tech, 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 September 9, 1993. Regulation: 8.