Abbott Globe Holder

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

510(k) Number

K832911 ↗

FDA Product Code

HJO

Device Class

Class II

Regulation

21 CFR Part 886.1850

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Clayman-Parel Capsule Coupeur

  Class I

  FDA 510(k) K841101 Active Cleared 16 May 1984

• Surgical Iop Monitor

  Class II

  FDA 510(k) K832996 Active Cleared 28 Nov 1983

• Rare-Earth Intra-Ocular Magnet

  Class I

  FDA 510(k) K831702 Active Cleared 30 Jun 1983

• Epa Automated Infusion Pole

  Class II

  FDA 510(k) K832997 Active Cleared 4 Oct 1983

• Gelender Vacuum Fixation Ring Sys

  Class I

  FDA 510(k) K832912 Active Cleared 10 Jan 1984