510(k) K974040 ยท FHA Clamp, Penile
C3 EXTERNAL MALE BLADDER CONTROL DEVICE
| Applicant | Timm Research Co., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Jul 14, 1998 |
| Received | Oct 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974040
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.