510(k) K831940 ยท FKQ System, Dialysate Delivery, Central Multiple Patient
GAMMA STERILIZED CAPILLARY FLOW DIALYZ
| Applicant | Travenol Laboratories, S.A., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 8, 1983 |
| Received | Jun 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831940
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.