510(k) K881062 ยท FJB Detector, Dialysate Level
CENTRY 2 ULTRAFILTRATION CONTROL KIT, #018762-002
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Apr 21, 1988 |
| Received | Mar 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881062
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.