510(k) K860368 ยท FFO Retractor, Self-Retaining
URDYN 5000 (UROFLOWMETER)
| Applicant | Dantec Electronics, Inc., Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 23, 1986 |
| Received | Feb 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860368
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.