SALTERLABS 8960 SERIES NEBULIZER (8960/8961/8966/8984)

SALTERLABS 8960 SERIES NEBULIZER (8960/8961/8966/8984) is an FDA 510(k)-cleared medical device (K961476) manufactured by Salter Labs. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1996. Regulation: 8.