
Fingerprint Bioteck, Inc.
Free shipping on orders over $99 · 30-day returns
FINGERPRINT-DOA is an FDA 510(k)-cleared medical device (K942836) manufactured by Fingerprint Bioteck, 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 April 30, 1995. Regulation: 8.