PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735)

PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735) is an FDA 510(k)-cleared medical device (K894230) manufactured by Siemens Medical Laboratories, 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 August 27, 1989. Regulation: 8.