510(k) K823522 ยท GKH Apparatus, Automated Blood Cell Diluting
DILULAB 230
| Applicant | Innovative Medical Systems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 28, 1982 |
| Received | Nov 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823522
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.