
Idaho Technology, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM is an FDA 510(k)-cleared medical device (K071188) manufactured by Idaho Technology, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 2007. Regulation: 8.