510(k) K061091 ยท KNG Monitor, Ultrasonic, Fetal
BABYBEAT CORDLESS
| Applicant | The Newman Group, LLC, Chicago IL, US |
| Decision | Substantially Equivalent, May 4, 2006 |
| Received | Apr 19, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061091
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.