510(k) K952274 ยท FMI Needle, Hypodermic, Single Lumen
CHEMOGUARD, P2 HIRISK
| Applicant | Biosafety Systems, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 29, 1995 |
| Received | May 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952274
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.