510(k) K131870 ยท OHT Light Based Over-The-Counter Hair Removal
GLIDE DEVICE
| Applicant | Home Skinovations , Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Aug 14, 2013 |
| Received | Jun 24, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131870
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.