
C.R. Bard, Inc.
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BUTTON REPLACEMENT GASTROSTOMY DEVICE is an FDA 510(k)-cleared medical device (K904779) manufactured by C.R. Bard, 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 January 17, 1991. Regulation: 8.