PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX

PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX is an FDA 510(k)-cleared medical device (K901141) manufactured by Baxter Healthcare Corp. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 8, 1990. Regulation: 8.