510(k) K936041 ยท FEN Device, Cystometric, Hydraulic
UROGRAM CYSTOMETROGRAM
| Applicant | Myo/Kinetic Systems, Inc., Menomonee Falls WI, US |
| Decision | Substantially Equivalent, Apr 18, 1994 |
| Received | Dec 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936041
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.