Nhs 2009SP Hearing Aid

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

510(k) Number

K911174 ↗

FDA Product Code

ESD

Device Class

Class I

Regulation

21 CFR Part 874.3300

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• Futura 67M, 68M, MEGAPOWERMP97, Integra 70, 71, 72, 73, Supra 51, 52, Supra 56, 57, 58, 59, Suprema 45, 46, 47, 48

  Class I

  FDA 510(k) K973861 Active Cleared 19 Nov 1997

• Nnhs 2050 Series (2055W-2054PP) Hearing Aids

  Class I

  FDA 510(k) K911182 Active Cleared 9 May 1991

• Magnatone Model M Prewired Faceplate Hearing Aid

  Class I

  FDA 510(k) K944241 Active Cleared 16 Nov 1994

• Model M Hearing Aid

  Class I

  FDA 510(k) K852656 Active Cleared 27 Dec 1985

• Interton Bte Hear Aid, Supra, Suprema, Minetta

  Class I

  FDA 510(k) K890525 Active Cleared 19 May 1989

• Magnatone / Sterling/ St; Magnatone/Db; Magnatone/ Liberty/ Lb; Magnatone/ Pearl/Ph C.I.C., S.P.I., One Touch, Designer

  Class I

  FDA 510(k) K973665 Active Cleared 4 Nov 1997

See all devices from Magnatone Hearing Aid Corp. →