Carrom Carelife Series 40000 Modular Bes System

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

510(k) Number

K854937 ↗

FDA Product Code

FNL

Device Class

Class II

Regulation

21 CFR Part 880.5100

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Centercom Control

  Class II

  FDA 510(k) K853270 Active Cleared 13 Nov 1985

• Everest & Jennings Tradition-Standard Bed L109684&

  Class II

  FDA 510(k) K854867 Active Cleared 4 Feb 1986

• Everest & Jennings Bed Model No. L109564 & L108564

  Class I

  FDA 510(k) K854776 Active Cleared 13 Dec 1985

• Everest & Jenning Series 5000 Modular Bed

  Class II

  FDA 510(k) K854832 Active Cleared 4 Feb 1986