510(k) K870860 ยท GKF Instrument, Hematocrit, Automated
CHEMPRO 1000(TM)
| Applicant | Arden Medical Systems, Inc., Arden Hills MN, US |
| Decision | Substantially Equivalent, Apr 14, 1987 |
| Received | Mar 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870860
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.