510(k) K983490 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
TERUMO VENOJECT,LUER ADAPTER
| Applicant | Terumo Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Nov 30, 1998 |
| Received | Oct 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983490
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.