
Amresco, Inc.
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AMRESCO SUBST CONCEN, PRO #2432,BUF,NAD,2455,TRI is an FDA 510(k)-cleared medical device (K852948) manufactured by Amresco, Inc.. 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 6, 1985. Regulation: 8.