
Carl Zeiss Meditec, Inc.
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GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIES is an FDA 510(k)-cleared medical device (K093213) manufactured by Carl Zeiss Meditec, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 11, 2010. Regulation: 8.