510(k) K946084 ยท FMI Needle, Hypodermic, Single Lumen
VANGUARD
| Applicant | Vanguard Container Corp., East Brunswick NJ, US |
| Decision | Substantially Equivalent, May 17, 1995 |
| Received | Dec 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946084
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.