510(k) K012879 ยท FPA Set, Administration, Intravascular
EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
| Applicant | Exelint Intl. Co., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jan 17, 2002 |
| Received | Aug 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012879
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.