
Bill Olson Corp.
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ZEFON BATERIAL/VIRAL FILTER is an FDA 510(k)-cleared medical device (K911651) manufactured by Bill Olson Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 29, 1991. Regulation: 8.

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