510(k) K924348 ยท HAW Neurological Stereotaxic Instrument
AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC
| Applicant | Ad-Tech Medical Instrument Corp, Racine WI, US |
| Decision | Substantially Equivalent, Nov 23, 1992 |
| Received | Aug 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924348
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.