LATEX CONDOMS - CODE NO. 404, NO. 424 & NO. 1000

LATEX CONDOMS - CODE NO. 404, NO. 424 & NO. 1000 is an FDA 510(k)-cleared medical device (K901669) manufactured by Allercare/Nsl, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 15, 1990. Regulation: 8.