C. R.Bard, Inc./Electrophysiology Division
6 FDA 510(k) clearances · Recalling firm
◉ Watch C. R.Bard, Inc./Electrophysiology Division
| Record | Firm | Date |
|---|---|---|
| Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 2 recall (Z-0598-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
| Bard Stinger M Ablation Catheters: Item Numbers 210001M 218501M 210002M 218502M 210003M 21 recall (Z-0599-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
| Bard Stinger S Ablation Catheter: Item Numbers 210001S 218501S 6210015S 210002S 218502S 62 recall (Z-0600-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
| Bard Stinger SM Ablation Catheter Item Numbers 210001SM 218501SM 210002SM 218502SM 210003S recall (Z-0601-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
| Bard Orbiter ST Artrial Mapping Steerable Catheter Item Numbers 320001 7FAM00001 7FAM00010 recall (Z-0602-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
| Bard Orbiter PV Steerable Catheter Item #: 320100 (Marketed in Europe Only) recall (Z-0603-03) | C. R.Bard, Inc./Electrophysiology Division | 2003-02-28 |
Track C. R.Bard, Inc./Electrophysiology Division automatically
Every clearance here is in the API, with alerts when new ones post.