510(k) K041358 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VENOJECT LUER ADAPTER
| Applicant | Terumo Europe N.V., Elkton MD, US |
| Decision | Substantially Equivalent, May 28, 2004 |
| Received | May 21, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041358
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.