
Fujirebio Diagnostics,Inc.
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Lumipulse G pTau217/ß-Amyloid 1-42 Plasma Ratio is an FDA 510(k)-cleared medical device (K242706) manufactured by Fujirebio Diagnostics,Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 15, 2025. Regulation: 8.