
The Perkin-Elmer Corp.
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SPECTROPHATOMETER MODELS 2280 & 2380AA is an FDA 510(k)-cleared medical device (K792557) manufactured by The Perkin-Elmer Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 15, 1980. Regulation: 8.