510(k) K980820 ยท HAW Neurological Stereotaxic Instrument
PHILIPS EASYGUIDE
| Applicant | Philips Medical Systems, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Oct 13, 1998 |
| Received | Mar 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980820
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.