510(k) K030671 ยท DQY Catheter, Percutaneous
MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MEDTRONIC 8F LAUNCHER BIOPSY CATHETER, MODEL LA8RVBB
| Applicant | Medtronic Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Jul 31, 2003 |
| Received | Mar 3, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030671
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.