
Tri-Med Specialties, Inc.
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E-Z P.E.G. W/PERCUTANEOUS ENDOSCOPY GASTROSTOMY is an FDA 510(k)-cleared medical device (K852535) manufactured by Tri-Med Specialties, 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 October 16, 1985. Regulation: 8.