GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR

GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR is an FDA 510(k)-cleared medical device (K952581) manufactured by Gamp & Assoc.. 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 January 4, 1996. Regulation: 8.