Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)

Q-TEL TELEMETRY SYSTEM V. 6.0 (ST) is an FDA 510(k)-cleared medical device (K992908) manufactured by Quinton, 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 March 5, 2000. Regulation: 8.