510(k) K991441 ยท KNG Monitor, Ultrasonic, Fetal
CADENCE DOPPLER ULTRASOUND SYSTEM
| Applicant | Medasonics, Inc., Sandy UT, US |
| Decision | Substantially Equivalent, Dec 28, 1999 |
| Received | Apr 26, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991441
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.