510(k) K030889 ยท MUI Media, Coupling, Ultrasound
ULTRAEKOGEL MODELS EK 2000 & EK 2001
| Applicant | Inmed Ltda., Alpharetta GA, US |
| Decision | Substantially Equivalent, May 23, 2003 |
| Received | Mar 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030889
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.