510(k) K874293 ยท KOD Catheter, Urological
ACKRAD V/CUG VOIDING CYSTOURETHROGRAPHY SET
| Applicant | Ackrad Laboratories, Cranford NJ, US |
| Decision | Substantially Equivalent, Dec 29, 1987 |
| Received | Oct 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874293
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.