510(k) K874602 ยท FMI Needle, Hypodermic, Single Lumen
ASD-BIO ANTI-STICK DEVICE
| Applicant | Biosurge, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Feb 19, 1988 |
| Received | Nov 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874602
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.