American Medical Devices, Inc.
ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT
SKU K970878UPC MPA
In Stock
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IIFDA 510(k) Cleared (K970878)
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Free shipping on orders over $99 · 30-day returns
American Medical Devices, Inc.
Free shipping on orders over $99 · 30-day returns
ENDOLIGHT FIBEROPTIC REGULAR MONOFILAMENT AND FINE MONOFILAMENT is an FDA 510(k)-cleared medical device (K970878) manufactured by American Medical Devices, Inc.. 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 May 5, 1997. Regulation: 8.
