Misonix, Inc. · Class II · Cleared Jul 9, 2008
| K-number | K070779 |
| Device name | SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM |
| Applicant | Misonix, Inc. |
| Product code | NTB |
| Device class | Class II |
| Decision date | Jul 9, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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