Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Techlab Inc., Corporate Research Center
Free shipping on orders over $99 · 30-day returns
GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK is an FDA 510(k)-cleared medical device (K103673) manufactured by Techlab Inc., Corporate Research Center. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 17, 2011. Regulation: 8.