
Uros Corp.
Free shipping on orders over $99 · 30-day returns
UROSPROBE SYSTEM, MODEL 1000 is an FDA 510(k)-cleared medical device (K960387) manufactured by Uros Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 31, 1996. Regulation: 8.