510(k) K930200 ยท KNG Monitor, Ultrasonic, Fetal
MULTI DOPPLEX II / FETAL DOPPLEX II
| Applicant | Huntleigh Healthcare, Inc., Eatontown NJ, US |
| Decision | Substantially Equivalent, Jun 24, 1994 |
| Received | Jan 14, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930200
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.