QUINTON 901 & 900 HOLTER SCANNER

QUINTON 901 & 900 HOLTER SCANNER is an FDA 510(k)-cleared medical device (K841611) 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 August 1, 1984. Regulation: 8.