510(k) K132616 ยท GWF Stimulator, Electrical, Evoked Response
EPAD
| Applicant | Safeop Surgical, Inc., Amherst MA, US |
| Decision | Substantially Equivalent, Jan 24, 2014 |
| Received | Aug 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132616
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.