
Bioject, Inc.
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BIOJECTOR 2000 MODEL 1B02000 is an FDA 510(k)-cleared medical device (K960373) manufactured by Bioject, 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 March 4, 1997. Regulation: 8.

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