BARRON MICROKERATOME SYSTEM, MODEL B2000

BARRON MICROKERATOME SYSTEM, MODEL B2000 is an FDA 510(k)-cleared medical device (K983317) manufactured by Barron Precision Instruments, LLC. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 1, 1998. Regulation: 8.