510(k) K201752 ยท HAW Neurological Stereotaxic Instrument
Disposable Pre-calibrated Suction
| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Jan 29, 2021 |
| Received | Jun 26, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201752
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.