510(k) K952573 ยท FEN Device, Cystometric, Hydraulic
RUSCH URODYNAMIC RECTAL BALLOON CATHETER
| Applicant | Rusch Intl., Jeffrey NH, US |
| Decision | Substantially Equivalent, Jun 15, 1995 |
| Received | Jun 5, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952573
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.