510(k) K130132 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
BABYLANCE HEEL INCISION DEVICE
| Applicant | Medipurpose Pte. , Ltd., Alpharetta GA, US |
| Decision | Substantially Equivalent, Feb 11, 2013 |
| Received | Jan 18, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130132
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.