Owen Mumford USA, Inc.
RAPPORT V.T.D.
SKU K982275UPC LKY
In Stock
—
IIFDA 510(k) Cleared (K982275)
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 (K982275) 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 December 3, 1998. Regulation: 8.
