510(k) K092364 ยท DTG Magnet, Test, Pacemaker
MODEL 220 PATIENT MAGNET
| Applicant | Cyberonics, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Nov 3, 2009 |
| Received | Aug 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092364
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.