| K-number | K953246 |
| Device name | OCTOROLL |
| Applicant | Octostop, Inc. |
| Product code | KXH |
| Device class | Class I |
| Decision date | Sep 29, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 892.1830 |
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