510(k) K883557 ยท GWQ Full-Montage Standard Electroencephalograph
NEUROWAVE SYSTEM 2
| Applicant | Durden Enterprises, Inc., Auburn GA, US |
| Decision | Substantially Equivalent, Dec 16, 1988 |
| Received | Aug 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883557
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.