510(k) K830999 ยท HAW Neurological Stereotaxic Instrument
DAP II BIOPSY GUIDE
| Applicant | Rapid Machine & Tool Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 12, 1983 |
| Received | Mar 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830999
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.