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Tester, Auditory Impedance

FDA product code ETY · Class 2 · Ear, Nose, Throat

244
Registered devices
6
Adverse events
1
Recalls
70
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2005-06-27Natus Medical IncInternal investigation revealed that Preamp cable assemblies in the device had not been properly tested, which could lead to potential shock to users.

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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.