510(k) K961834 ยท HAW Neurological Stereotaxic Instrument
PHILIPS EASYGUIDE NEURO
| Applicant | Philips Medical Systems, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Nov 8, 1996 |
| Received | May 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961834
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.