510(k) K190250 ยท HAW Neurological Stereotaxic Instrument
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| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Sep 6, 2019 |
| Received | Feb 7, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190250
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.