510(k) K991601 ยท DQY Catheter, Percutaneous
DUAL LUMEN CATHETER, MODEL DL-35-90
| Applicant | Endologix, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 28, 1999 |
| Received | May 10, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991601
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.