510(k) K880391 ยท EXQ Cystometer, Electrical Recording
DACOMED CYSTOMETER
| Applicant | Dacomed Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 27, 1988 |
| Received | Jan 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880391
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.