510(k) K873348 ยท GGK Products, Red-Cell Lysing Products
CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.
| Applicant | Abbott Diagnostics, Mountain View CA, US |
| Decision | Substantially Equivalent, Sep 9, 1987 |
| Received | Aug 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873348
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.