510(k) K230201 ยท HAW Neurological Stereotaxic Instrument
Disposable Pre-calibrated Brain Biopsy Needle 2.0
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, Feb 22, 2023 |
| Received | Jan 25, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230201
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.