510(k) K082935 ยท DQX Wire, Guide, Catheter
VISION WIRE CORONARY GUIDEWIRE
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Dec 4, 2008 |
| Received | Oct 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082935
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.