
Sanarus Medical, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000 is an FDA 510(k)-cleared medical device (K052861) manufactured by Sanarus Medical, Inc.. 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 November 14, 2005. Regulation: 8.