510(k) K900482 ยท GWF Stimulator, Electrical, Evoked Response
SOFTWARE & HARDWARE ADDITION TO SENTINEL-4 EEG
| Applicant | Axon Systems, Inc., Hauppauge NY, US |
| Decision | Substantially Equivalent, Jun 20, 1990 |
| Received | Feb 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900482
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.