510(k) K141242 ยท OHT Light Based Over-The-Counter Hair Removal
GLIDE DEVICE
| Applicant | Home Skinovations , Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Oct 17, 2014 |
| Received | May 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141242
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.