Ethicon Endo-Surgery, LLC
Endopath Electrosurgery Probe Plus II
SKU K180031UPC GEI
In Stock
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IIFDA 510(k) Cleared (K180031)
1
Free shipping on orders over $99 · 30-day returns
Ethicon Endo-Surgery, LLC
Free shipping on orders over $99 · 30-day returns
Endopath Electrosurgery Probe Plus II is an FDA 510(k)-cleared medical device (K180031) manufactured by Ethicon Endo-Surgery, LLC. 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 May 6, 2018. Regulation: 8.
