
Organon Teknika Corp.
Free shipping on orders over $99 · 30-day returns
NEPHROSS ALLEGRO H.F. is an FDA 510(k)-cleared medical device (K844748) manufactured by Organon Teknika Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 1985. Regulation: 8.