
Bio-Plexus, Inc.
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BIO-PLEXUS NEEDLE DISPOSAL CONTAINER is an FDA 510(k)-cleared medical device (K960933) manufactured by Bio-Plexus, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 1996. Regulation: 8.

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