510(k) K131040 ยท FMI Needle, Hypodermic, Single Lumen
EXTAVIPRO STERICAN 30G
| Applicant | B.Braun Melsungen AG, Fredrichsdorf, DE |
| Decision | Substantially Equivalent, Jul 15, 2013 |
| Received | Apr 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131040
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.