510(k) K940203 ยท FEN Device, Cystometric, Hydraulic
TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
| Applicant | Life-Tech Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, Mar 30, 1994 |
| Received | Jan 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940203
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.