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Medisiss
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MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K042659) manufactured by Medisiss. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 13, 2005. Regulation: 8.

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