Hearing Aid Danavox 775V

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K790539 ↗

FDA Product Code

ESD

Device Class

Class I

Regulation

21 CFR Part 874.3300

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Hearing Aid, Model 781

  Class I

  FDA 510(k) K781881 Active Cleared 15 Nov 1978

• In-The-Ear Model 101M

  Class I

  FDA 510(k) K812939 Active Cleared 6 Nov 1981

• Behind-The-Ear #123 Agci

  Class I

  FDA 510(k) K832326 Active Cleared 29 Sep 1983

• Behind-The-Ear Model 115

  Class I

  FDA 510(k) K812937 Active Cleared 6 Nov 1981

• Perceptor

  Class I

  FDA 510(k) K770321 Active Cleared 28 Feb 1977

• Hearing Aid Model 775

  Class I

  FDA 510(k) K771607 Active Cleared 25 Aug 1977

See all devices from Danavox, Inc. →