PRO-VENT, LINE DRAW, PULSATOR

PRO-VENT, LINE DRAW, PULSATOR is an FDA 510(k)-cleared medical device (K952516) manufactured by Smiths Industries Medical Systems, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 1995. Regulation: 8.