510(k) K113332 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
ON CALL CHOSEN LANCING DEVICE
| Applicant | ACON Laboratories, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Apr 18, 2012 |
| Received | Nov 14, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K113332
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.