510(k) K894389 ยท GGX Pipette, Sahli
CREATININE FOR MANUAL OR AUTOMATED APPLICATIONS
| Applicant | Catachem, Inc., Port Chester NY, US |
| Decision | Substantially Equivalent, Oct 12, 1989 |
| Received | Jul 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894389
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.