510(k) K132613 ยท OHS Light Based Over The Counter Wrinkle Reduction
SONILASE LIGHT THERAPY DEVICE
| Applicant | Biorenew Labs, LLC, Coralville IA, US |
| Decision | Substantially Equivalent, Feb 5, 2014 |
| Received | Aug 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132613
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.