510(k) K840384 ยท HHI System, Abortion, Vacuum
DIAGNOSTIC DILATATION & MENSTRUAL KIT
| Applicant | Intl. Medical Technologies, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 30, 1984 |
| Received | Jan 30, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840384
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.