Owen Mumford USA, Inc.
RAPPORT V.T.D.
SKU K971443UPC LKY
In Stock
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IIFDA 510(k) Cleared (K971443)
1
Free shipping on orders over $99 · 30-day returns
Owen Mumford USA, Inc.
Free shipping on orders over $99 · 30-day returns
RAPPORT V.T.D. is an FDA 510(k)-cleared medical device (K971443) manufactured by Owen Mumford USA, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 25, 1997. Regulation: 8.
