Middle Ear Analyzer (Imped. Audiomtr)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K790846 ↗

FDA Product Code

EWO

Device Class

Class II

Regulation

21 CFR Part 874.1050

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Middle Ear Analyzer (Impedance Audiometer)

  Class II

  FDA 510(k) K863353 Active Cleared 3 Nov 1986

• Middle Ear Analyzer (Impedance Audio

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  FDA 510(k) K820715 Active Cleared 9 Apr 1982

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  Class II

  FDA 510(k) K870030 Active Cleared 13 Mar 1987

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  Class II

  FDA 510(k) K193033 Active Cleared 24 Apr 2020

• Gsi SA60 Dpoae System

  Class II

  FDA 510(k) K970324 Active Cleared 6 Jun 1997

See all devices from Grason-Stadler, Inc. →