510(k) K162067 ยท HKX Tonometer, Ac-Powered
VX130 Ophthalmic Diagnostic Device
| Applicant | Luneau Sas, Prunay Le Gillon, FR |
| Decision | Substantially Equivalent, Apr 24, 2017 |
| Received | Jul 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162067
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.