THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER)

THORNTON TITANIUM SPECULUM (MODIFIED BARRAQUER) is an FDA 510(k)-cleared medical device (K863989) manufactured by Keeler Instruments, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 30, 1986. Regulation: 8.