510(k) K131905 ยท MUI Media, Coupling, Ultrasound
SOLID GEL PAD
| Applicant | Bluemtech, Anaheim CA, US |
| Decision | Substantially Equivalent, Jul 18, 2013 |
| Received | Jun 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131905
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.