510(k) K863609 ยท FKP System, Dialysate Delivery, Single Patient
SINGLE-PATIENT AUTOMATIC DIALYSIS UNIT MOD. DBB-22
| Applicant | International Medical Products, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 25, 1987 |
| Received | Sep 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863609
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.