
Consumer Sensory Products, Inc.
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CONSUMER SENSORY PRODUCTS BIO-LOG 8000 is an FDA 510(k)-cleared medical device (K904955) manufactured by Consumer Sensory Products, 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 April 24, 1991. Regulation: 8.

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