510(k) K193539 ยท MUU System, Suction, Lipoplasty
REVOLVE ENVI 600 Advanced Adipose System
| Applicant | Lifecell Corporation, Branchburg NJ, US |
| Decision | Substantially Equivalent, May 28, 2020 |
| Received | Dec 20, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193539
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.