510(k) K981619 ยท FMI Needle, Hypodermic, Single Lumen
VACUETTE MULTIPLE SAMPLE LUER ADAPTER
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Jul 15, 1998 |
| Received | May 6, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981619
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.