510(k) K213519 ยท GYD Transducer, Tremor
Rune Labs Tremor Transducer System
| Applicant | Rune Labs, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Jun 10, 2022 |
| Received | Nov 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213519
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.