
Hollister, Inc.
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HOLLISTER(R) BEDSIDE DRAINAGE COLLECTION SYST 9878 is an FDA 510(k)-cleared medical device (K926570) manufactured by Hollister, 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 May 20, 1993. Regulation: 8.