NZD

1 FDA 510(k) clearances · Product code

FDA profile

Official device name

Stretcher, Patient Restraint

Device class

Class I (low risk)

Regulation

21 CFR 880.6900

Medical specialty

General Hospital

Flags

GMP exempt

FDA definition

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

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