
Ameditech, Inc.
Free shipping on orders over $99 · 30-day returns
AMEDITECH DRUGSMARTCUP is an FDA 510(k)-cleared medical device (K053175) manufactured by Ameditech, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 7, 2005. Regulation: 8.