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Device, Vein Location, Liquid Crystal

FDA product code KZA · Class 1 · General Hospital

14
Registered devices
19
Adverse events
2
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.

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