
Zimmer Patient Care Division
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GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS is an FDA 510(k)-cleared medical device (K935709) manufactured by Zimmer Patient Care Division. 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 January 30, 1994. Regulation: 8.