510(k) K802887 ยท GWQ Full-Montage Standard Electroencephalograph
MODEL EEG 4221
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Dec 16, 1980 |
| Received | Nov 17, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802887
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.