510(k) K833320 ยท KEA Resins, Ion-Exchange
AMBERLITE CG50 RESIN, 100-200 MESH
| Applicant | Biosan Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1983 |
| Received | Sep 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833320
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.