PHILIPS MULTI LEAF PRESCRIPTION ENTRY SYSTEM (MLP)

PHILIPS MULTI LEAF PRESCRIPTION ENTRY SYSTEM (MLP) is an FDA 510(k)-cleared medical device (K953570) manufactured by Philips Medical Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 24, 1995. Regulation: 8.