510(k) K032141 ยท FMI Needle, Hypodermic, Single Lumen
SECUMAX BLOOD COLLECTION SYSTEM
| Applicant | Tiger Meditech Incorporated, Columbus OH, US |
| Decision | Substantially Equivalent, Jan 28, 2004 |
| Received | Jul 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032141
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.