510(k) K901670 ยท HAW Neurological Stereotaxic Instrument
GNOMOS STEREOTACTIC DEVICE
| Applicant | Medical Equipment Development Co., Inc., Cinnaminson NJ, US |
| Decision | Substantially Equivalent, Jul 3, 1990 |
| Received | Apr 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901670
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.