510(k) K092192 ยท HAW Neurological Stereotaxic Instrument
WAYPOINT STEREOTACTIC SYSTEM
| Applicant | FHC, Inc., Bowdoin ME, US |
| Decision | Substantially Equivalent, Feb 12, 2010 |
| Received | Jul 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092192
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.