510(k) K884183 ยท DQX Wire, Guide, Catheter
BURRON TEFLON-COATED GUIDEWIRE
| Applicant | Burron Medical, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Aug 3, 1989 |
| Received | Oct 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884183
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.