PARAMAX(R) ELECTROLYTE CALIBRATOR 1&2/MODIFICATION

PARAMAX(R) ELECTROLYTE CALIBRATOR 1&2/MODIFICATION is an FDA 510(k)-cleared medical device (K910309) manufactured by Baxter Healthcare Corp. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 1991. Regulation: 8.