510(k) K935456 ยท HAW Neurological Stereotaxic Instrument
REGULUS MEASUREMENT UNIT
| Applicant | Compass Intl., Inc., Rochester MN, US |
| Decision | Substantially Equivalent, Oct 13, 1995 |
| Received | Nov 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935456
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.