
Eidolon Corp.
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EIDOLON ENDOSCOPE COUPLER is an FDA 510(k)-cleared medical device (K942141) manufactured by Eidolon Corp.. 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 26, 1994. Regulation: 8.