FOUR MODIFICATIONS TO OPHTHALAS ARGON/DYE LASER

FOUR MODIFICATIONS TO OPHTHALAS ARGON/DYE LASER is an FDA 510(k)-cleared medical device (K881494) manufactured by Biophysic Medical, 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 August 29, 1988. Regulation: 8.