510(k) K102637 ยท MUI Media, Coupling, Ultrasound
DYNAREX ULTRASOUND GEL
| Applicant | Dynarex Corporation, Orangeburg NY, US |
| Decision | Substantially Equivalent, Feb 16, 2011 |
| Received | Sep 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102637
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.