510(k) K031894 ยท MUI Media, Coupling, Ultrasound
SCANTEC PAD
| Applicant | Sonotech, Inc., Bellingham WA, US |
| Decision | Substantially Equivalent, Jul 18, 2003 |
| Received | Jun 19, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031894
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.