DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER

DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER is an FDA 510(k)-cleared medical device (K871149) manufactured by Iontec Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 4, 1987. Regulation: 8.