Morrison Medical Stretcher/Cot and Backboard Restraints

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K963399 ↗

FDA Product Code

FMQ

Device Class

Class I

Regulation

21 CFR Part 880.6760

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Morrison Medical Disposable Restraint Strap

  Class I

  FDA 510(k) K963494 Active Cleared 6 Nov 1996

• Cinch Strap with Buckle

  Class I

  FDA 510(k) K963370 Active Cleared 8 Nov 1996

• Best Strap Restraint

  Class I

  FDA 510(k) K963371 Active Cleared 7 Nov 1996

• Ankle Restraint System

  Class I

  FDA 510(k) K963416 Active Cleared 6 Nov 1996

• Deluxe Limb Restraint with Double D-Ring and Strap Deluxe Limb Restraint with Strap

  Class I

  FDA 510(k) K963387 Active Cleared 8 Nov 1996

• Torso/Waist Restraint

  Class I

  FDA 510(k) K963374 Active Cleared 8 Nov 1996

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