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Beckman Coulter, Inc. · Model OSR61155 · UDI-DI 15099590011468

JHY Prescription
1
510(k) clearances
51
Adverse events
2
Recalls
11
Facilities

Description

CK-MB

Recalls

DateFirmReason
2018-01-02Siemens Healthcare Diagnostics, Inc.Concentrations for the level of biotin that does not interfere is not currently listed in the instruction for use for the Dimension Vista CTNI, Dimension Vista MMB, Dimension Sirol
2010-12-22BioCheck IncProduct labels indicate that the products are for IVD use and they do not have an approved 510(k).

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.