510(k) K880892 ยท FMI Needle, Hypodermic, Single Lumen
BLOOD COLLECTING NEEDLE AND HOLDERS
| Applicant | Abco Dealers, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 21, 1988 |
| Received | Mar 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880892
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.