MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX

MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX is an FDA 510(k)-cleared medical device (K954492) manufactured by Mercury Medical. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 20, 1996. Regulation: 8.