510(k) K850425 ยท KZM Device, Muscle Monitoring
DENTAL ANESTHESIA APPARATUS
| Applicant | Pain Prevention, Inc., Chicago IL, US |
| Decision | Substantially Equivalent for Some Indications, Oct 9, 1986 |
| Received | Feb 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850425
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.