510(k) K960503 ยท FEN Device, Cystometric, Hydraulic
DANTEC DUET
| Applicant | Dantec Medical, Inc., Allendale NJ, US |
| Decision | Substantially Equivalent, Sep 16, 1996 |
| Received | Feb 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960503
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.