| K-number | K000070 |
| Device name | FLOCATH |
| Applicant | Rusch Intl. |
| Product code | KOD |
| Device class | Class II |
| Decision date | Feb 18, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 876.5130 |
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