Interacoustics Ep 15 Abr Stand Alone Unit

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K991853 ↗

FDA Product Code

GWJ

Device Class

Class II

Regulation

21 CFR Part 882.1900

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Interacoustics Model AD226 Diagnostic Audiometer

  Class II

  FDA 510(k) K981327 Active Cleared 11 May 1998

• Interacoustics AT22T Automatic Impedance Audiometer

  Class II

  FDA 510(k) K990585 Active Cleared 17 May 1999

• Interacoustics Model AD229 Diagnostic Audiometer

  Class II

  FDA 510(k) K982249 Active Cleared 7 Aug 1998

• Interacoustics Model AZ26 Clinical Impedance Audiometer

  Class II

  FDA 510(k) K990652 Active Cleared 17 May 1999

• Interacoustics Model Mt 10, Handheld Impedance Audiometer

  Class II

  FDA 510(k) K983832 Active Cleared 25 Jan 1999