| K-number | K093810 |
| Device name | BF-NAVI |
| Applicant | Kgt, Inc. |
| Product code | JAK |
| Device class | Class II |
| Decision date | Jun 18, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 892.1750 |
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