DeviceClearance

Product code NZD— General Hospital

PEDI-SPIDER STRAP

Classification name
Stretcher, Patient Restraint
Device class
Class 1
Regulation
21 CFR 880.6900
Advisory panel
General Hospital
Total cleared
1
First cleared
Most recent

FDA classification definition

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

— U.S. Food and Drug Administration, device classification record for product code NZD under 21 CFR 880.6900, via openFDA

Market context for product code NZD

FDA has cleared 1 device under product code NZD, all in 2006, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code NZD

Recent clearances under product code NZD

Data sourced from openFDA. This site is unofficial and independent of the FDA.