510(k) K801629 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter
COVER-ALL MALE INCONTINENCE DEVICE
| Applicant | The Urology Group, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 12, 1980 |
| Received | Jul 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801629
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.