Nuvasive, Inc. · Class II · Cleared May 14, 2010
| K-number | K094054 |
| Device name | MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE |
| Applicant | Nuvasive, Inc. |
| Product code | GWF |
| Device class | Class II |
| Decision date | May 14, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 882.1870 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov