510(k) K882064 ยท FMI Needle, Hypodermic, Single Lumen
LO-CORE NEEDLE
| Applicant | Device Labs, Inc., Medway MA, US |
| Decision | Substantially Equivalent, Jul 8, 1988 |
| Received | May 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882064
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.