510(k) K110241 ยท DQX Wire, Guide, Catheter
ENDOLOGIX GUIDEWIRE
| Applicant | Techdevice Corporation, Watertown MA, US |
| Decision | Substantially Equivalent, Feb 25, 2011 |
| Received | Jan 27, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110241
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.