Kowa Co. , Ltd. · Class II · Cleared Jan 16, 2009
| K-number | K083387 |
| Device name | MODIFICATION TO KOWA NONMYD ALPHA-DIII |
| Applicant | Kowa Co. , Ltd. |
| Product code | HKI |
| Device class | Class II |
| Decision date | Jan 16, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 886.1120 |
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