510(k) K884620 ยท FMI Needle, Hypodermic, Single Lumen
ASD SINGLE LUMEN NEEDLE
| Applicant | Biosurge, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Nov 21, 1988 |
| Received | Nov 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884620
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.