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Parker Quality & Compliance

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Device type

Flow Cytometric Test System For Hematopoietic Neoplasms

Product code PWD · Class II · 21 CFR 864.7010 · Hematology

Reagents intended for in vitro diagnostic use as a panel for qualitative identification of cell populations by multiparameter immunophenotyping on a flow cytometer. These reagents are used as an aid in the differential diagnosis of hematologically abnormal patients having, or suspected of having the following hematopoietic neoplasms: chronic leukemia, acute leukemia, non-Hodgkin's lymphoma, myeloma, myelodysplastic syndrome (MDS), and/or myeloproliferative neoplasms (MPN)

FDA classification database

Recent 510(k)s

Recent recalls

No recalls in the archive for PWD.