510(k) K113533 ยท HAE Rongeur, Manual
NEURO CHECK DEVICE WITH IO-FLEX WIRE
| Applicant | Baxano, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Apr 11, 2012 |
| Received | Nov 30, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113533
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.