510(k) K100470 ยท DQX Wire, Guide, Catheter
GTX 12 GIDEWIRE
| Applicant | Medtronic, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Apr 21, 2010 |
| Received | Feb 18, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100470
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 15, 2013 | Medtronic Vascular ProVia CROSSING GUIDEWIRE; Models: 15PROV300HS, 3PROV180HS, 3PROV180SS, 3PROV300HS, 3PROV300SS, 9PROV180HS, 9PROV180SS
Medtronic guide wires are steerable guide wires that are used for the introduct Terminated |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.