BUEHLMANN LAB AS, ACE ANGIO CONV ENZYME KIN ASSAY

BUEHLMANN LAB AS, ACE ANGIO CONV ENZYME KIN ASSAY is an FDA 510(k)-cleared medical device (K913091) manufactured by American Laboratory Products Co., Ltd.. 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 August 25, 1991. Regulation: 8.