
Superior Biosystems, Inc.
Free shipping on orders over $99 · 30-day returns
NO. 87500-NUPORT PEG GASTROSTOMY TUBE KIT 22 FR is an FDA 510(k)-cleared medical device (K894653) manufactured by Superior Biosystems, 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 December 20, 1989. Regulation: 8.