510(k) K103095 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON
| Applicant | Medtronic, Ireland, Santa Rosa CA, US |
| Decision | Substantially Equivalent, Oct 22, 2010 |
| Received | Oct 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103095
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.