510(k) K020390 ยท LQK Home Uterine Activity Monitor
MODIFICATION TO FETAL ASSIST
| Applicant | Huntleigh Diagnostics , Ltd., Eatontown NJ, US |
| Decision | Substantially Equivalent, Apr 19, 2002 |
| Received | Feb 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020390
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.