510(k) K042373 ยท DQX Wire, Guide, Catheter
GALEO FOCUS GUIDE WIRE
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Mar 2, 2005 |
| Received | Sep 1, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042373
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.