510(k) K141713 ยท MUU System, Suction, Lipoplasty
SMARTGRAFT 200 SYSTEM
| Applicant | Ingeneron, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Oct 28, 2014 |
| Received | Jun 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141713
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.