FDA 510(k) Applications for Medical Device Product Code: NZD (Stretcher, Patient Restraint)

FDA 510(k) Applications for Medical Device Product Code "NZD"
(Stretcher, Patient Restraint)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K061721	EMERGENCY PRODUCTS AND RESEARCH	PEDI-SPIDER STRAP	08/17/2006