510(k) K910733 ยท FMI Needle, Hypodermic, Single Lumen
MEDISYSTEMS ANTI-STICK INJECTION SITE NEEDLE
| Applicant | Medisystems Corp., San Francisco CA, US |
| Decision | Substantially Equivalent, Jun 6, 1991 |
| Received | Feb 21, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910733
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.