510(k) K823760 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
PRICK-TEST NEEDLE
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jan 14, 1983 |
| Received | Dec 14, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823760
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.