MOD. 9542 FLOW-THRU INJECT. TEMP. SENSOR

MOD. 9542 FLOW-THRU INJECT. TEMP. SENSOR is an FDA 510(k)-cleared medical device (K801552) manufactured by Edwards Laboratories. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 27, 1980. Regulation: 8.