510(k) K203712 ยท LQZ Device, Jaw Repositioning
The Slide
| Applicant | Biotex, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jul 20, 2021 |
| Received | Dec 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203712
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.