SALTERLABS 8660 SERIES NEBULIZER

SALTERLABS 8660 SERIES NEBULIZER is an FDA 510(k)-cleared medical device (K962879) 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 October 21, 1996. Regulation: 8.