510(k) K031222 ยท MUI Media, Coupling, Ultrasound
SCANLUBE
| Applicant | Sonotech, Inc., Bellingham WA, US |
| Decision | Substantially Equivalent, Jul 23, 2003 |
| Received | Apr 17, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031222
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.