Gn Resound A/S · Class II · Cleared Mar 13, 2008
| K-number | K073636 |
| Device name | TINNITUS SOUND GENERATOR MODULE |
| Applicant | Gn Resound A/S |
| Product code | KLW |
| Device class | Class II |
| Decision date | Mar 13, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 874.3400 |
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