510(k) K873569 ยท FMI Needle, Hypodermic, Single Lumen
BLOOD NEEDLE HOLDER
| Applicant | Sage Products, Inc., Cary IL, US |
| Decision | Substantially Equivalent, Nov 3, 1987 |
| Received | Sep 2, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873569
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.