510(k) K830001 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
SUPERJET BTD BLEEDING TIME DEVICE DISP
| Applicant | Medprobe Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1983 |
| Received | Jan 3, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830001
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.