510(k) K810115 ยท KNG Monitor, Ultrasonic, Fetal
DOPPLEX-PLB & PXB
| Applicant | Huntleigh Technology, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 16, 1981 |
| Received | Jan 16, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810115
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.