510(k) K920574 ยท EXQ Cystometer, Electrical Recording
CAMSYS 6300
| Applicant | F.M. Wiest USA, Inc., Oradell NJ, US |
| Decision | Substantially Equivalent, Feb 17, 1993 |
| Received | Feb 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920574
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.