Conmed Corporation
BEAMER ARGON PROBE
SKU K081644UPC GEI
In Stock
—
IIFDA 510(k) Cleared (K081644)
1
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Conmed Corporation
Free shipping on orders over $99 · 30-day returns
BEAMER ARGON PROBE is an FDA 510(k)-cleared medical device (K081644) manufactured by Conmed Corporation. 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 September 9, 2008. Regulation: 8.
