Syntheon, LLC
ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL
SKU K080317UPC FDF
In Stock
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IIFDA 510(k) Cleared (K080317)
1
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Syntheon, LLC
Free shipping on orders over $99 · 30-day returns
ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL is an FDA 510(k)-cleared medical device (K080317) manufactured by Syntheon, LLC. 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 April 28, 2008. Regulation: 8.
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