510(k) K994358 ยท DQX Wire, Guide, Catheter
ATW MARKER WIRE STEERABLE GUIDEWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jan 13, 2000 |
| Received | Dec 27, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K994358
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.