Livewire™
Steerable Electrophysiology Catheter
Who Else Makes It
Concentrated in Jiangsu (2), Tianjin (1), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jiangyin Sinbon Electronics Co Ltd | Jiangyin | Jiangsu | Contract manufacturer | 13 |
| Palconn Technology Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 2 |
| Steris Sterilization Technologies (Suzhou) Ltd | Suzhou | Jiangsu | Contract manufacturer | 44 |
| Tianjin Ethylene Oxide Sterilization Technology Co., Ltd. | Tianjin | Tianjin | Contract manufacturer | 4 |
| Shanghai Microport EP Medtech Co., Ltd. | Shanghai | Shanghai | Manufacturer | 3 |
Record
| Listed by | St. Jude Medical, United States |
|---|---|
| FDA product code | DRF |
| Device type | Catheter, Electrode Recording, Or Probe, Electrode Recording |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1220 |
| Establishment | Manufacturer, Exporter |
| 510(k) | K101955 |
| Record published | 2015-03-05 |
| Record revised | 2023-11-01 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: STORE IN COOL, DARK, DRY PLACE AWAY FROM RADIATION. |
| Sizes | Catheter gauge 5 to 7 Fr; length 1.7 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 401908 | Catheter Gauge 7 Fr | In distribution |
| 401904 | Catheter Gauge 7 Fr | In distribution |
| 401905 | Catheter Gauge 7 Fr | In distribution |
| 401781 | Catheter Gauge 5 Fr | In distribution |
| 401780 | Catheter Gauge 5 Fr | In distribution |
| 402023 | Catheter Gauge 5 Fr | In distribution |
| 401932 | Catheter Gauge 7 Fr | In distribution |
| D402058 | Catheter Gauge 6 Fr | In distribution |
| 401914 | Catheter Gauge 7 Fr | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Map-iT | Access Point Medical, LLC | 420 |
| Woven | Boston Scientific Corporation | 126 |
| Inquiry™ | Irvine Biomedical. Inc. | 122 |
| Webster | Biosense Webster, Inc. | 121 |
| Viking™ | Boston Scientific Corporation | 81 |
| EasyFinder Fixed Curve Diagnostic Catheter | Shanghai Microport EP Medtech Co., Ltd. | 56 |
| Supreme™ | St. Jude Medical Cardiovascular Division | 55 |
| Celsius | Biosense Webster, Inc. | 47 |
| Response™ | St. Jude Medical Cardiovascular Division | 46 |
| Torqr™ | Medtronic, Inc. | 32 |
| Catheter, Electrode Recording, Or Probe, Electrode Recording | Medtronic, Inc. | 27 |
| Lasso NAV | Biosense Webster, Inc. | 22 |
Showing 12 of 112. All products under Catheter, Electrode Recording, Or Probe, Electrode Recording
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K160335 | 2016-12-13 |
| K151622 | 2015-07-15 |
| K150631 | 2015-04-01 |
| K120544 | 2012-03-19 |
| K102721 | 2010-10-18 |
| K101955 | 2010-10-15 |
| K101623 | 2010-08-13 |
| K081803 | 2009-05-13 |
| K080179 | 2009-01-07 |
| K072012 | 2007-08-22 |
| K062251 | 2006-10-20 |
| K022380 | 2002-10-01 |
| K011766 | 2001-07-03 |
| K002976 | 2000-12-22 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2014-10-14 | Class II | Labeling mix-ups | St. Jude Medical is performing a voluntary recall of batch 4671318, model number 401353 of the Response Fixed Curve DECA 6F 65cm CSL 2/8 Catheter. Specifically, the firm has identified that every device packaged within batch 4671318 contain | 26 | 2014-12-10 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P950005 | 2001-10-05 | CELSIUS DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER | Biosense Webster, Inc. |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.