
World of Medicine Lemke GmbH
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SIGHTFIX is an FDA 510(k)-cleared medical device (K024251) manufactured by World of Medicine Lemke GmbH. 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 March 17, 2003. Regulation: 8.

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