Emergency/Accident Trolley 550

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

510(k) Number

K946101 ↗

FDA Product Code

FPO

Device Class

Class II

Regulation

21 CFR Part 880.6910

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Intergrated Monitoring Archiving and Communications Systems (Imacs)

  Class II

  FDA 510(k) K941762 Active Cleared 22 Feb 1995

• I.m Probes

  Class I

  FDA 510(k) K802951 Active Cleared 17 Dec 1980

• Cardiolipin G EIA Test System

  Class II

  FDA 510(k) K946215 Active Cleared 24 Jan 1996

• Cardiolipin a Eia Test System

  Class II

  FDA 510(k) K946216 Active Cleared 24 Jan 1996

• Redfield Infrared Coagulator

  Class II

  FDA 510(k) K950836 Active Cleared 24 Mar 1995

• Coopersurgical Infrared Coagulator

  Class II

  FDA 510(k) K974168 Active Cleared 23 Jan 1998

See all devices from Hogan & Hartson →

• What is the Emergency/Accident Trolley 550 used for?

  The Emergency/Accident Trolley 550 is a wheeled stretcher designed for transporting patients during emergency or accident situations within general hospital settings. It facilitates patient movement in healthcare facilities during critical situations.

• Is the Emergency/Accident Trolley 550 single-use or reusable?

  The device is supplied as a single unit, but the provided data does not specify whether it is intended for single-use or multiple reuse. This information should be confirmed with the manufacturer for proper usage guidelines.

• What regulatory approvals does the Emergency/Accident Trolley 550 have?

  The Emergency/Accident Trolley 550 has received FDA 510(k) clearance as a Class II medical device. It was determined to be substantially equivalent to other legally marketed devices and is intended for general hospital use.

• Are there any specific storage requirements for the Emergency/Accident Trolley 550?

  No specific storage requirements are mentioned in the authorization data for the Emergency/Accident Trolley 550. Standard medical device storage practices would likely apply, but users should consult the manufacturer's instructions for any specific guidance.