The following data is part of a premarket notification filed by Barrx Medical Inc with the FDA for Halo Ablation Catheter Model 90-9100, Halo90 Ultra Ablation Catheter Model 90-9200.
| Device ID | K101111 |
| 510k Number | K101111 |
| Device Name: | HALO ABLATION CATHETER MODEL 90-9100, HALO90 ULTRA ABLATION CATHETER MODEL 90-9200 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BARRX MEDICAL INC 540 OAKMEAD PARKWAY Sunnyvale, CA 94085 |
| Contact | Viorica Filimon |
| Correspondent | Viorica Filimon BARRX MEDICAL INC 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 | 2010-04-21 |
| Decision Date | 2010-06-18 |
| Summary: | summary |