510(k) K880373 ยท GKF Instrument, Hematocrit, Automated
IONOMETER E-HK AND ACCESSORIES
| Applicant | Smash Ent., Inc., Arden Hills MN, US |
| Decision | Substantially Equivalent, Mar 17, 1988 |
| Received | Jan 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880373
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.