BEECHER 20 GA. PROBE

BEECHER 20 GA. PROBE is an FDA 510(k)-cleared medical device (K833800) manufactured by Beecher Medical Diagnostic Instrumentation. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 3, 1984. Regulation: 8.