510(k) K023143 ยท KNG Monitor, Ultrasonic, Fetal
ECHO SOUNDER, ES-102EX
| Applicant | Koven Technology, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Dec 19, 2002 |
| Received | Sep 20, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023143
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.