510(k) K030779 ยท DQY Catheter, Percutaneous
5F MEDTRONIC LAUNCHER GUIDE CATHETER
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Apr 24, 2003 |
| Received | Mar 11, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030779
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 1, 2006 | Medtronic, Inc. CATHETER LA5IMAA 5F 110CM
Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH.GUIDE 5F JL 4.0 110CM
CATHETER LA5JL40A LA 5F 110CM JL40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coro Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH.GUIDE 5F JR 4.0 110CM
CATHETER LA5JR40A LA 5F 110CM JR4.0 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coro Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH GUIDE 5F SR3.0 LAUNCHER
CATHETER LA5SR30 LA 5F 100CM SR30 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coro Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH GUIDE 5F SR3.5 LAUNCHER
CATHETER LA5SR35 LA 5F 100CM SR35 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coro Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH GUIDE 5F SR4.0 LAUNCHER
CATHETER LA5SR40 LA 5F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coro Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. CATH.GUIDE 5F SR 5.0 110CM
CATHETER LA5SR50A LA 5F 110CM SR5 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the corona Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.