510(k) K885323 ยท FHA Clamp, Penile
DACOMED EXTERNAL MALE CONTINENCE DEVICE
| Applicant | Dacomed Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Dec 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885323
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.