510(k) K894930 ยท ETN Stimulator, Nerve
DENTEC 4000
| Applicant | Dentec, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Mar 27, 1990 |
| Received | Aug 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894930
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.