510(k) K211691 ยท MUI Media, Coupling, Ultrasound
Ultrast Gel
| Applicant | Ultrast, Inc., Oceanside NY, US |
| Decision | Substantially Equivalent, Dec 22, 2021 |
| Received | Jun 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211691
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.