Symbiosis Corp.
GASTRO ENTEROLOGICAL BIOPTOME
SKU K894419UPC KNW
In Stock
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IIFDA 510(k) Cleared (K894419)
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Free shipping on orders over $99 · 30-day returns
Symbiosis Corp.
Free shipping on orders over $99 · 30-day returns
GASTRO ENTEROLOGICAL BIOPTOME is an FDA 510(k)-cleared medical device (K894419) manufactured by Symbiosis Corp.. 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 September 7, 1989. Regulation: 8.
