510(k) K043249 ยท FMI Needle, Hypodermic, Single Lumen
ATRION NEEDLEVISE LARGE-BORE SHARPS SECURING DEVICE
| Applicant | Atrion Medical Products, Inc., Arab AL, US |
| Decision | Substantially Equivalent, May 25, 2005 |
| Received | Nov 23, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043249
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.