510(k) K781521 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter
CUTTER RESIFLEX URINE METER
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 22, 1978 |
| Received | Sep 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781521
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.