510(k) K061908 ยท GWQ Full-Montage Standard Electroencephalograph
NICOLETONE SYSTEM V32 AMPLIFIER
| Applicant | Viasys Neuro Care, Stoughton WI, US |
| Decision | Substantially Equivalent, Nov 6, 2006 |
| Received | Jul 5, 2006 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K061908
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.