510(k) K972469 ยท FMI Needle, Hypodermic, Single Lumen
SELFSHIELD HN SELF SHEATHING HYPODERMIC NEEDLE
| Applicant | Beech Medical Products, Inc., Middlesex NJ, US |
| Decision | Substantially Equivalent, Aug 27, 1997 |
| Received | Jul 1, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972469
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.