510(k) K861560 ยท FMI Needle, Hypodermic, Single Lumen
MEDIPOINT MULTI-SAMPLE BLOOD COLLECTING NEEDLE
| Applicant | Medi Point, Inc., Mineola NY, US |
| Decision | Substantially Equivalent, May 12, 1986 |
| Received | Apr 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861560
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.