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Lipoprotein, Low Density, Removal
FDA product code MMY · Class 3 · Unknown
27
Registered devices
42
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
B.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGTUBING SYSTEM FOR PLASMAPHERESIS — KANEKA PHARMA AMERICA LLCB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGTUBING SYSTEM FOR PLASMAPHERESIS — KANEKA PHARMA AMERICA LLCB.BRAUN — B.Braun Avitum AGH.E.L.P.® — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGLIPOSORBER — KANEKA CORPORATIONH.E.L.P.® — B.Braun Avitum AGH.E.L.P.® — B.Braun Avitum AGB.BRAUN — B.Braun Avitum AGAPHERESIS MACHINE — KANEKA PHARMA AMERICA LLCSULFLUX — KANEKA PHARMA AMERICA LLCH.E.L.P.® — B.Braun Avitum AG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-02-17 | Kaneka America Corp | Labeling change to due to the risk of severe anaphylactoid reactions including shock in patients treated with the Liposorber LA-15 LDL Adsorption Column under c |
| 2006-07-06 | Wako Chemicals, USA Inc | Unexpected low cholesterol results-The Cholesterol calibrator (Lp(a)) component of the in vitro diagnostic kit for cholesterol testing, has provided patient res |
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