510(k) K790025 ยท KSF Kit, Quality Control For Blood Banking Reagents
COUNTER CHECK, H001, H002, H003
| Applicant | Diagnostic Technology, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1979 |
| Received | Jan 3, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790025
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.