510(k) K131842 ยท FMI Needle, Hypodermic, Single Lumen
STERICAN CANNULA
| Applicant | B.Braun Medical, Inc., Allentown PA, US |
| Decision | Substantially Equivalent, Aug 20, 2013 |
| Received | Jun 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131842
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.