510(k) K102328 ยท FMI Needle, Hypodermic, Single Lumen
BLUNT FILL NEEDLE AND BLUNT PLASTIC CANNULA
| Applicant | Shandong Weigao Group Medical Polymer Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, May 13, 2011 |
| Received | Aug 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102328
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.