510(k) K920737 ยท FMI Needle, Hypodermic, Single Lumen
LIFESHIELD VIAL ADAPTER
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Dec 15, 1992 |
| Received | Feb 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920737
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.