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Cancer Monitoring Test System, Soluble Mesothelin-Related Peptides, Epithelioid/Biphasic Mesothelioma

FDA product code OAW · Class f · Unknown

3
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

MESOMARK — Fujirebio Diagnostics, Inc.Lumipulse G Mesothelin Immunoreaction Cartridges — FUJIREBIO INC.Lumipulse G Mesothelin Calibrator — FUJIREBIO INC.

Recent recalls

DateFirmReason
2010-07-29Fujirebio Diagnostics, Inc.presence of material attached to the bottom of some wells in places visible to the naked eye, which caused an overestimation of the sample.

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