510(k) K130518 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MINI-MIDLINE EXTENDED DWELL SAFETY CATHETER
| Applicant | Luther Needlesafe Products, Inc., Mission Viejo CA, US |
| Decision | Substantially Equivalent, Apr 30, 2013 |
| Received | Feb 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130518
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.