| K-number | K913020 |
| Device name | BIODEX SYSTEM 2,MODEL S2-S |
| Applicant | Biodex Corp. |
| Product code | IKK |
| Device class | Class II |
| Decision date | Oct 3, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 890.1925 |
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