
KARL STORZ Endoscopy-America, Inc.
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KARL STORZ URETERO-RENOSCOPE/URETERSCOPE is an FDA 510(k)-cleared medical device (K940464) 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 June 23, 1994. Regulation: 8.