510(k) K820173 ยท FIF Set, Dialysis, Single Needle With Uni-Directional Pump
COBE SINGLE-NEEDLE CONTROLLER #18-756
| Applicant | Cobe Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 23, 1982 |
| Received | Jan 21, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820173
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.