510(k) K172358 ยท LKX Device, Thermal, Hemorrhoids
Instalief
| Applicant | Privi Medical Pte, Ltd., Singapore, SG |
| Decision | Substantially Equivalent, Jan 10, 2018 |
| Received | Aug 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172358
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.