Uromed Corp.
MODIFICATION TO CAVERMAP SURGICAL AID
SKU K010213UPC ETN
In Stock
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IIFDA 510(k) Cleared (K010213)
1
Free shipping on orders over $99 · 30-day returns
Uromed Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO CAVERMAP SURGICAL AID is an FDA 510(k)-cleared medical device (K010213) manufactured by Uromed Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 2001. Regulation: 8.
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