510(k) K010958 ยท FMI Needle, Hypodermic, Single Lumen
FISTULOK FISTULA NEEDLE PROTECTION
| Applicant | Diasol, Inc., North Hollywood CA, US |
| Decision | Substantially Equivalent, May 18, 2001 |
| Received | Mar 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010958
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.