The following data is part of a premarket notification filed by Barrx Medical, Incorporated with the FDA for Barrx Models Halo360 And Halo360+ Coagulation Catheters.
| Device ID | K080557 |
| 510k Number | K080557 |
| Device Name: | BARRX MODELS HALO360 AND HALO360+ COAGULATION CATHETERS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BARRX MEDICAL, INCORPORATED 540 OAKMEAD PARKWAY Sunnyvale, CA 94085 |
| Contact | Viorica Filimon |
| Correspondent | Viorica Filimon BARRX MEDICAL, INCORPORATED 540 OAKMEAD PARKWAY Sunnyvale, CA 94085 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-02-28 |
| Decision Date | 2008-04-02 |
| Summary: | summary |