510(k) K971719 ยท DQX Wire, Guide, Catheter
THEROX INFUSION GUIDEWIRES
| Applicant | Therox, Inc., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Nov 3, 1997 |
| Received | May 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971719
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.