510(k) K820625 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
HEMALET AUTOMATIC LANCET DEVICE
| Applicant | Medprobe Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 9, 1982 |
| Received | Mar 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820625
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.