
Plexus Medical
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PLEXUS/3000 (P/3000), PLEXUS/3500 (P/3500) is an FDA 510(k)-cleared medical device (K952610) manufactured by Plexus Medical. 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 September 12, 1995. Regulation: 8.

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