JACKSON ESOPHAGEAL DILATOR

JACKSON ESOPHAGEAL DILATOR is an FDA 510(k)-cleared medical device (K990935) manufactured by Pilling Weck Surgical. 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 May 16, 1999. Regulation: 8.