MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS

MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS is an FDA 510(k)-cleared medical device (K922996) manufactured by Chiron Vision Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 26, 1992. Regulation: 8.