510(k) K092923 ยท MUU System, Suction, Lipoplasty
CYTORI PUREGRAFT 250/PURE SYSTEM
| Applicant | Cytori Therapeutics, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 6, 2010 |
| Received | Sep 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092923
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.