| K-number | K875205 |
| Device name | TRI-FLOW CATHETER |
| Applicant | Neurodynamics, Inc. |
| Product code | JXG |
| Device class | Class II |
| Decision date | May 31, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 882.5550 |
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