DATEX-OHMEDA 3800+/3800P+ OR 3900/3900P PULSE OXIMETERS

DATEX-OHMEDA 3800+/3800P+ OR 3900/3900P PULSE OXIMETERS is an FDA 510(k)-cleared medical device (K983684) manufactured by Datex-Ohmeda, 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 November 5, 1998. Regulation: 8.