MODELS 706 ECG/PRESSURE/RESP./SAO2, 705 ECG/RESP.

MODELS 706 ECG/PRESSURE/RESP./SAO2, 705 ECG/RESP. is an FDA 510(k)-cleared medical device (K901504) manufactured by Ivy Biomedical Systems, 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 August 22, 1990. Regulation: 8.