FDA Device Intelligence
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Dialyzer Reprocessing System

FDA product code LIF · Class 2 · Gastroenterology, Urology

14
Registered devices
137
Adverse events
1
Recalls
57
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2009-04-21Hach CoSome of the reagent strip bottles contain the incorrect strips

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.