Product code
NZD: Stretcher, patient restraint
FDA product code · Class I · General Hospital
Key facts
| Product code | NZD |
|---|---|
| Device | Stretcher, patient restraint |
| Device class | Class I |
| Regulation number | 880.6900 |
| Review panel | General Hospital |
| Medical specialty | General Hospital |
| Submission type | 510(K) Exempt |
| GMP exempt | Yes |
| Definition | Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations. |
At a glance
- 1–9 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 10–99 UDI devices (GUDID)
- 1–9 MAUDE adverse event reports
- 1–9 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database