KEELER TEARSCOPE-PLUS

KEELER TEARSCOPE-PLUS is an FDA 510(k)-cleared medical device (K973064) manufactured by Keeler Instruments, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 6, 1998. Regulation: 8.