510(k) K992598 ยท KOI Stimulator, Nerve, Peripheral, Electric
TOF-WATCH SX
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Aug 30, 1999 |
| Received | Aug 3, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992598
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.