510(k) K926088 ยท FEN Device, Cystometric, Hydraulic
FST CATH UD-DUAL DUAL PRESSURE CATHETER
| Applicant | Fiberoptic Sensor Technlogies, Inc., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Jun 18, 1993 |
| Received | Dec 2, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926088
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.