Ultra-Wide Safety Spectacle Frame

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

510(k) Number

K813156 ↗

FDA Product Code

HQZ

Device Class

Class I

Regulation

21 CFR Part 886.5842

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Zee Manual Resuscitator

  Class II

  FDA 510(k) K812022 Active Cleared 31 Jul 1981

• Zee Surgical Instruments

  Class I

  FDA 510(k) K812814 Active Cleared 6 Nov 1981

• Zee Life Support Air Pants

  Class II

  FDA 510(k) K812564 Active Cleared 23 Oct 1981

• Zee Electrode-Gel

  Class II

  FDA 510(k) K812284 Active Cleared 8 Sep 1981

• Zee Extrication Device

  Class I

  FDA 510(k) K812342 Active Cleared 21 Sep 1981

• Zee Sphygmomanometer

  Class II

  FDA 510(k) K823501 Active Cleared 21 Jan 1983

See all devices from Zee Medical Products Co., Inc. →