Olympus Corporation
OLYMPUS ENDOARM
SKU K043128UPC GWG
In Stock
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IIFDA 510(k) Cleared (K043128)
1
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Olympus Corporation
Free shipping on orders over $99 · 30-day returns
OLYMPUS ENDOARM is an FDA 510(k)-cleared medical device (K043128) manufactured by Olympus Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 2004. Regulation: 8.
