
InBios International, Inc.
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Active Anthrax DetectTM Plus Rapid Test is an FDA 510(k)-cleared medical device (DEN220044) manufactured by InBios International, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 2, 2023. Regulation: 8.