KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR

KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR is an FDA 510(k)-cleared medical device (K931313) manufactured by Konica Medical Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 6, 1993. Regulation: 8.