
Wako Chemicals USA, Inc.
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WAKO L-TYPE FE, WAKO L-TYPE CALIBRATOR is an FDA 510(k)-cleared medical device (K984119) manufactured by Wako Chemicals USA, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 14, 1999. Regulation: 8.