510(k) K930171 ยท FEN Device, Cystometric, Hydraulic
FST DUAL, DUAL PRESSURE URODYNAMICS MONITOR
| Applicant | Fiberoptic Sensor Technlogies, Inc., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Nov 4, 1993 |
| Received | Jan 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930171
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.