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Endocare, Inc.
Free shipping on orders over $99 · 30-day returns
ENDOCARE PERCUTANEOUS ACCESS SET is an FDA 510(k)-cleared medical device (K002396) manufactured by Endocare, 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 October 12, 2000. Regulation: 8.

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