510(k) K820568 ยท DZM Needle, Dental
MUSCLE DYSFUNCTION MONITOR
| Applicant | A Company, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 9, 1982 |
| Received | Mar 2, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820568
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.