510(k) K032411 ยท DQX Wire, Guide, Catheter
JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE
| Applicant | Js Vascular, Inc., Orinda CA, US |
| Decision | Substantially Equivalent, Oct 7, 2003 |
| Received | Aug 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032411
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.