510(k) K945820 ยท LQZ Device, Jaw Repositioning
DESRA
| Applicant | D.S.R.A., Inc., East Lansing MI, US |
| Decision | Substantially Equivalent, Jun 15, 1995 |
| Received | Nov 28, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945820
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.