INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT

INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT is an FDA 510(k)-cleared medical device (K902628) manufactured by Biometric Research Institute, 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 February 24, 1991. Regulation: 8.