510(k) K121839 ยท DQY Catheter, Percutaneous
UNBALLOON NON-OCCLUSIVE MODELING CATHETER
| Applicant | LeMaitre Vascular, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Aug 8, 2012 |
| Received | Jun 22, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121839
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.