LIFELINE(R) PERSONAL RESPONSE SYSTEM

LIFELINE(R) PERSONAL RESPONSE SYSTEM is an FDA 510(k)-cleared medical device (K914103) manufactured by Lifeline Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 26, 1991. Regulation: 8.