510(k) K972538 ยท FMI Needle, Hypodermic, Single Lumen
FLOW-EZE BLUNT CANNULA (1999BC)
| Applicant | Acacia, Inc., Ojai CA, US |
| Decision | Substantially Equivalent, Jul 15, 1998 |
| Received | Jul 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972538
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.