510(k) K170363 ยท OMC Reduced- Montage Standard Electroencephalograph
Ceribell Pocket EEG Device
| Applicant | Ceribell, Inc., Mountainview CA, US |
| Decision | Substantially Equivalent, May 8, 2017 |
| Received | Feb 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170363
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.