Sanarus Medical, Inc.
MODIFICATION TO SANARUS VISICA TREATMENT SYSTEM
SKU K021211UPC GEH
In Stock
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IIFDA 510(k) Cleared (K021211)
1
Free shipping on orders over $99 · 30-day returns
Sanarus Medical, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO SANARUS VISICA TREATMENT SYSTEM is an FDA 510(k)-cleared medical device (K021211) 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 June 25, 2002. Regulation: 8.
