510(k) K223577 ยท HAW Neurological Stereotaxic Instrument
Localite TMS Navigator TS
| Applicant | Localite GmbH, Bonn, DE |
| Decision | Substantially Equivalent, Apr 17, 2023 |
| Received | Nov 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223577
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.