Acclarent, Inc. · Class II · Cleared Apr 1, 2011
| K-number | K103595 |
| Device name | ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM |
| Applicant | Acclarent, Inc. |
| Product code | ETD |
| Device class | Class II |
| Decision date | Apr 1, 2011 |
| Decision | Substantially Equivalent |
| Regulation | 874.3880 |
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