510(k) K121849 ยท DWM Apparatus, Suction, Patient Care
PLEURX PLEURAL CATHETER SYSTEM, PLEURX CATHETER ACCESS KIT, PLEURX CATHETER INSERTION STYLET, PLEURX INTEGRAL VALVED PEE
| Applicant | Care Fusion, Waukegan IL, US |
| Decision | Substantially Equivalent, Oct 18, 2012 |
| Received | Jun 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121849
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.