KARL STORZ ADAPTERS FOR DOCUMENTATION PURPOSES

KARL STORZ ADAPTERS FOR DOCUMENTATION PURPOSES is an FDA 510(k)-cleared medical device (K950336) manufactured by KARL STORZ Endoscopy-America, 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 February 12, 1995. Regulation: 8.