510(k) K141749 ยท FMI Needle, Hypodermic, Single Lumen
CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT
| Applicant | Facet Technologies, LLC, Kennesaw GA, US |
| Decision | Substantially Equivalent, Jul 29, 2014 |
| Received | Jun 30, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141749
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.