510(k) K020921 ยท FMI Needle, Hypodermic, Single Lumen
NO-POKES NEEDLE SAFETY DEVICE
| Applicant | Bemis Mfg. Co., Sheboygan Falls WI, US |
| Decision | Substantially Equivalent, Jul 11, 2002 |
| Received | Mar 21, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020921
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.