| K-number | K011308 |
| Device name | MULTISTIM |
| Applicant | Pajunk GmbH |
| Product code | BXN |
| Device class | Class II |
| Decision date | Nov 29, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 868.2775 |
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