PROSPECTOR PLUS (CODE NAME : RD-0508)

PROSPECTOR PLUS (CODE NAME : RD-0508) is an FDA 510(k)-cleared medical device (K973881) manufactured by J.F. Jelenko & Co., Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 23, 1997. Regulation: 8.