510(k) K113255 ยท MUU System, Suction, Lipoplasty
PUREGRAFT 850/PURE SYSTEM
| Applicant | Cytori Therapeutics, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 7, 2012 |
| Received | Nov 3, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113255
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.