SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER

SALTER LABS SINGLE PATIENT USE EXHALATION AEROSOL FILTER is an FDA 510(k)-cleared medical device (K992986) 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 September 23, 1999. Regulation: 8.