NZD

Stretcher, Patient Restraint

Product code

NZD

Device name

Stretcher, Patient Restraint

Device class

Class 1

21 CFR

21 CFR 880.6900

Medical specialty

General Hospital

Marketing pathway

510(K) Exempt

Flag

GMP exempt

510(k) clearances (all years, FDA)

1 (all years; only the last 3 years are listed here)

FDA classification definition

Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations.

Definition text from the FDA device classification database (U.S. federal government work, public domain).