510(k) K042224 ยท KDN System, Perfusion, Kidney
RM3 RENAL PRESERVATION SYSTEM
| Applicant | Waters Instruments, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 22, 2004 |
| Received | Aug 17, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042224
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.