MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEM

MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEM is an FDA 510(k)-cleared medical device (K970964) manufactured by International Imaging Electronics. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 12, 1997. Regulation: 8.