PHILIPS BV 300 SERIES

PHILIPS BV 300 SERIES is an FDA 510(k)-cleared medical device (K953910) manufactured by Philips Medical Systems North America, 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 17, 1995. Regulation: 8.