Barrx Medical, Incorporated · Class II · Cleared Apr 2, 2008
| K-number | K080557 |
| Device name | BARRX MODELS HALO360 AND HALO360+ COAGULATION CATHETERS |
| Applicant | Barrx Medical, Incorporated |
| Product code | GEI |
| Device class | Class II |
| Decision date | Apr 2, 2008 |
| Decision | Substantially Equivalent |
| Regulation | — |
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