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Device, Nerve Conduction Velocity Measurement

FDA product code JXE · Class 2 · Neurology

205
Registered devices
93
Adverse events
1
Recalls
27
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-04-18Biomet, Inc.Incorrect product picture label was on the product box.

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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.