510(k) K082511 ยท FMI Needle, Hypodermic, Single Lumen
MEDIGARD BLOOD COLLECTION DEVICE
| Applicant | Medigard Limited, Crofton MD, US |
| Decision | Substantially Equivalent, Jan 16, 2009 |
| Received | Aug 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082511
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.