510(k) K220231 ยท LXV Apparatus, Vestibular Analysis
GyroStim
| Applicant | Ultrathera Technologies, Inc., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Apr 27, 2022 |
| Received | Jan 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220231
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.