
Fujirebio Diagnostics,Inc.
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Lumipulse G whole PTH is an FDA 510(k)-cleared medical device (K190702) manufactured by Fujirebio Diagnostics,Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 29, 2019. Regulation: 8.