KARL STORZ Endoscopy-America, Inc.
MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR
SKU K062464UPC GEI
In Stock
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IIFDA 510(k) Cleared (K062464)
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Free shipping on orders over $99 · 30-day returns
KARL STORZ Endoscopy-America, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR is an FDA 510(k)-cleared medical device (K062464) manufactured by KARL STORZ Endoscopy-America, Inc.. 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 February 15, 2007. Regulation: 8.
