APNEA ALARM FOR ADULT-PEDIATRIC & NEON

APNEA ALARM FOR ADULT-PEDIATRIC & NEON is an FDA 510(k)-cleared medical device (K831601) manufactured by Plasmedics, 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 September 25, 1983. Regulation: 8.