# Stretcher, Patient Restraint
> **Product code: NZD** · Class I — Low Risk (general controls) · General Hospital · 21 CFR 880.6900
## Classification
- **FDA Product Code:** NZD
- **Device class:** Class I — Low Risk (general controls)
- **Regulation:** 21 CFR 880.6900
- **Review panel:** HO
- **Medical specialty:** General Hospital
- **Submission type:** 4
- **GMP exempt:** Y
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

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

## Market data
- **Cleared 510(k) submissions:** 1
- **Registered establishments:** 60
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=NZD)
---
*AI Analytics · CC0 1.0*