
KARL STORZ Endoscopy-America, Inc.
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KARL STORZ BOUGIES AND DILATORS is an FDA 510(k)-cleared medical device (K950125) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 6, 1995. Regulation: 8.