510(k) K972698 ยท KOI Stimulator, Nerve, Peripheral, Electric
TOF-WATCH
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Dec 16, 1997 |
| Received | Jul 18, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972698
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.