MODIFIED ASSESS(R) PEAK FLOW METER

MODIFIED ASSESS(R) PEAK FLOW METER is an FDA 510(k)-cleared medical device (K902292) manufactured by Health Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 9, 1990. Regulation: 8.