510(k) K881654 ยท FMI Needle, Hypodermic, Single Lumen
ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE
| Applicant | Medical Safety Products, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Jul 8, 1988 |
| Received | Apr 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881654
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.