510(k) K182211 ยท GWG Endoscope, Neurological
Aurora Surgiscope System
| Applicant | Rebound Therapeutics Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Jan 18, 2019 |
| Received | Aug 15, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182211
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.