510(k) K850169 ยท FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable
ERIS URO-DIAGNOSTIC SYSTEM
| Applicant | Eris Medical Technology, New Providence NJ, US |
| Decision | Substantially Equivalent, Apr 22, 1985 |
| Received | Jan 16, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850169
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.