510(k) K041665 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
L1-PRO SYSTEM
| Applicant | Pelikan Technologies, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 23, 2004 |
| Received | Jun 18, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041665
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.