510(k) K080300 ยท NUV Massager, Vacuum, Light Induced Heating
CUTERA MULTIMODAL CELLULITE PRODUCT (CMMCD)
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Apr 8, 2008 |
| Received | Feb 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080300
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.