510(k) K905641 ยท FEN Device, Cystometric, Hydraulic
FST CATH-UD CATHETER
| Applicant | Fiberoptic Sensor Technlogies, Inc., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Feb 19, 1991 |
| Received | Dec 18, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905641
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.