Product code
GWW: Ataxiagraph
FDA product code · Class I · Neurology
Key facts
| Product code | GWW |
|---|---|
| Device | Ataxiagraph |
| Device class | Class I |
| Regulation number | 882.1030 |
| Review panel | Neurology |
| Medical specialty | Neurology |
| Submission type | 510(K) Exempt |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Exemption is limited to devices that do not provide an interpretation or a clinical implication of the measurement. |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 1–9 UDI devices (GUDID)
- 1–9 MAUDE adverse event reports
- None 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