FDA 510(k) Applications Submitted by VIORICA FILIMON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060169 |
01/23/2006 |
BARRX HALO COAGULATION SYSTEM, BARRX HALO COAGULATION GENERATOR, BARRX COAGULATION CATHETER, MODELS 2200-115A, 1520F |
BARRX MEDICAL, INCORPORATED |
| K080557 |
02/28/2008 |
BARRX MODELS HALO360 AND HALO360+ COAGULATION CATHETERS |
BARRX MEDICAL, INCORPORATED |
| K101111 |
04/21/2010 |
HALO ABLATION CATHETER MODEL 90-9100, HALO90 ULTRA ABLATION CATHETER MODEL 90-9200 |
BARRX MEDICAL INC |
| K071543 |
06/05/2007 |
HALO360' COAGULATION CATHETER |
BARRX MEDICAL, INCORPORATED |
| K062225 |
08/02/2006 |
HALO COAGULATION CATHETER |
BARRX MEDICAL, INCORPORATED |
| K082202 |
08/05/2008 |
HALO360 ENERGY GENERATOR, MODELS 1100C-115B AND 1100C-230B |
BARRX MEDICAL, INCORPORATED |
| K092487 |
08/13/2009 |
HALOFLEX ENERGY GENERATOR, MODELS 1190A-115A AND 1190A-230A |
BARRX MEDICAL, INCORPORATED |
| K062723 |
09/12/2006 |
HALO90 COAGULATION CATHETER |
BARRX MEDICAL, INCORPORATED |
| K093008 |
09/28/2009 |
HALO ABLATION CATHETER, MODEL 90-9100 |
BARRX MEDICAL, INCORPORATED |
| K083711 |
12/15/2008 |
MODIFICATION TO: HALO COAGULATION CATHETER, MODELS 32041-18, 32041-20, 32041-22, 32041-25, 32041-28, 32041-31, 32041-34 |
BARRX MEDICAL, INCORPORATED |
| K083737 |
12/16/2008 |
HALO ABLATION CATHETER |
BARRX MEDICAL, INCORPORATED |
| K093855 |
12/16/2009 |
HALO 360 & SIZING BALLOON, MODEL 3441C |
BARRX MEDICAL, INCORPORATED |
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