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

Bayer Corp.
Free shipping on orders over $99 · 30-day returns
BAYER DIAGNOSTICS ADVIA CENTAUR TOXOPLASMA IGM ASSAY is an FDA 510(k)-cleared medical device (K010755) manufactured by Bayer Corp.. 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 19, 2001. Regulation: 8.