Skip to content

Hare Folding Back Emergency Stretcher

by Dyna Corp. 510(k)

Active United States

510(k) K902503

Overview

The Hare Folding Back Emergency Stretcher is a wheeled stretcher designed for emergency medical use. It is classified as a Class II medical device and is intended for use in general hospital settings.

This stretcher is manufactured by Dyna Corp. and was FDA 510(k) cleared on June 26, 1990, with product code FPO. The device is substantially equivalent to other wheeled stretchers and is regulated under number 880.6910.

AI-generated from registry data, 26 Sep 2026.Not verified by deviCERTS or the manufacturer

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK902503 Date26 Jun 1990ClearedStatusActive

Coverage

1 jurisdiction

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
FPO
Device Class
Class II
Regulation
21 CFR Part 880.6910
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Other devices from Dyna Corp.

Questions

  • What is the Hare Folding Back Emergency Stretcher used for?

    The Hare Folding Back Emergency Stretcher is designed for emergency medical use in general hospital settings. It is a wheeled stretcher that allows for patient transport and is classified as a Class II medical device.

  • Is the Hare Folding Back Emergency Stretcher single-use or reusable?

    The device data does not specify whether the Hare Folding Back Emergency Stretcher is single-use or reusable. As a Class II medical device intended for hospital settings, it is likely designed for multiple uses, but this information is not explicitly stated in the provided data.

  • What is the regulatory status of the Hare Folding Back Emergency Stretcher?

    The Hare Folding Back Emergency Stretcher was FDA 510(k) cleared on June 26, 1990, with product code FPO. It is classified as a Class II medical device and is substantially equivalent to other wheeled stretchers, regulated under number 880.6910.

  • Who manufactures the Hare Folding Back Emergency Stretcher?

    The Hare Folding Back Emergency Stretcher is manufactured by Dyna Corp., located at 6300 Yarrow Dr., Carlsbad, CA 92009. The contact person listed is Richard A. Yeager.