510(k) K091670 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER
| Applicant | Becton, Dickinson & CO, Sandy UT, US |
| Decision | Substantially Equivalent, Jul 1, 2009 |
| Received | Jun 9, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091670
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.