NZD — Stretcher, Patient Restraint Class I

FDA Device Classification

Classification Details

Product Code
NZD
Device Class
Class I
Regulation Number
880.6900
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Definition

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K061721emergency products and researchPEDI-SPIDER STRAPAugust 17, 2006