
Bard Peripheral Vascular, Inc.
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BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT is an FDA 510(k)-cleared medical device (K133948) manufactured by Bard Peripheral Vascular, 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 February 20, 2014. Regulation: 8.