510(k) K000310 ยท HAW Neurological Stereotaxic Instrument
VOYAGER 6.0 SOFTWARE OPTION
| Applicant | Philips Medical Systems (Cleveland), Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Feb 15, 2000 |
| Received | Feb 1, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000310
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.