510(k) K080360 ยท DQY Catheter, Percutaneous
ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER
| Applicant | Endologix, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 8, 2008 |
| Received | Feb 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080360
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.